- Research article
- Open Access
- Open Peer Review
Protective effect of KCNH2 single nucleotide polymorphism K897T in LQTS families and identification of novel KCNQ1 and KCNH2mutations
- Xianqin Zhang†1, 2,
- Shenghan Chen†2,
- Li Zhang3,
- Mugen Liu2,
- Sharon Redfearn4,
- Randall M Bryant4,
- Carlos Oberti2,
- G Michael Vincent3 and
- Qing K Wang1, 2Email author
© Zhang et al; licensee BioMed Central Ltd. 2008
- Received: 16 March 2008
- Accepted: 23 September 2008
- Published: 23 September 2008
KCNQ1 and KCNH2 are the two most common potassium channel genes causing long QT syndrome (LQTS), an inherited cardiac arrhythmia featured by QT prolongation and increased risks of developing torsade de pointes and sudden death. To investigate the disease expressivity, this study aimed to identify mutations and common variants that can modify LQTS phenotype.
In this study, a cohort of 112 LQTS families were investigated. Among them two large LQTS families linkage analysis with markers spanning known LQTS genes was carried out to identify the specific gene for mutational analysis. All exons and exon-intron boundaries of KCNH2 and KCNQ1 were sequenced for mutational analysis.
LQTS-associated mutations were identified in eight of 112 families. Two novel mutations, L187P in KCNQ1 and 2020insAG in KCNH2, were identified. Furthermore, in another LQTS family we found that KCNH2 mutation A490T co-segregated with a common SNP K897T in KCNH2. KCNH2 SNP K897T was reported to exert a modifying effect on QTc, but it remains controversial whether it confers a risk or protective effect. Notably, we have found that SNP K897T interacts with mutation A490T in cis orientation. Seven carriers for A490T and the minor allele T of SNP K897T showed shorter QTc and fewer symptoms than carriers with A490T or A490P (P < 0.0001).
Our family-based approach provides support that KCNH2 SNP K897T confers a protective effect on LQTS patients. Our study is the first to investigate the effect of SNP K897T on another KCNH2 mutation located in cis orientation. Together, our results expand the mutational and clinical spectrum of LQTS and provide insights into the factors that determine QT prolongation associated with increased risk of ventricular tachycardia and sudden death.
- Mutation Carrier
- Mutation A490T
- L187P Mutation
- LQTS Patient
- KCNH2 Gene
Long QT syndrome (LQTS) is an inheritable cardiac ion channelopathy characterized by prolonged QT intervals and characteristic T wave morphology changes on electrocardiograms (ECG). Patients with LQTS have increased risks of developing life-threatening polymorphic ventricular tachycardia/fibrillation (VT/VF) when subjected to physical or emotional stress, or upon exposure to QT prolonging drugs. VT/VF can result in cardiac events such as syncope, cardiac arrest and sudden death . LQTS-related cardiac events often occur in the young, otherwise healthy individuals, and sudden death may present as the first symptom in many cases.
Multiple genes have been found to cause LQTS and these include KCNQ1 (LQT1), KCNH2 (LQT2), SCN5A (LQT3), ANK2 (LQT4), KCNE1 (LQT5), KCNE2 (LQT6), KCNJ2 (LQT7), CACNA1C (LQT8), CAV3 (LQT9) and SCNB4 (LQT10). LQT4-10 are rare and there is a controversy as whether some of the subtypes are truly LQTS. LQT1 and LQT2 remain the mainstay as the most common LQTS genotypes. Previously, we reported a study of mutational analysis of KCNQ1 in 102 families and patients with a family history of lethal cardiac events, including LQTS . The present study was carried out as a continued investigation in the same cohort of patients plus 10 new LQTS families/patients enrolled since the earlier report, and focused on mutational analysis of the KCNQ1 gene in the new families/patients and the LQT2 gene, KCNH2 in the whole cohort. Multiple mutations were identified. Most importantly, we provide the first family-based genetic evidence to show that two variants in KCNH2, mutation A490T and a common single nucleotide polymorphism (SNP) K897T, interact with each other in cis orientation to reduce the risk of LQTS (shorter QTc, less severe symptoms).
Patients with a clinical diagnosis of LQTS or idiopathic VT/VF and their first degree blood related family members were enrolled from medical clinics in North America. A total 154 families/patients were involved in this study. This study was approved by the Cleveland Clinic Foundation Institutional Review Board on Human Subject Research and informed consent was obtained from the study participants or their guardians.
Diagnosis of LQTS was based on the QT interval and T wave morphology from 12-lead ECG and medical history of syncope, cardiac arrest and sudden death as described previously [3–7]. All the 12-lead ECG tracings available to the study were recorded at 25 mm/sec as standard in North America. QT interval was manually measured in leads II or V5 or the lead with longest QT interval and QTc was calculated using Bazett's formula for heart rate correction. A LQTS clinical diagnosis was considered if QTc ≥ 0.47 s in males or QTc ≥ 0.48 s in females . Borderline QT prolongation (0.45–0.47 s) associated with symptoms were also considered as affected. Asymptomatic family members with QTc of ≤0.44 s and with a normal T wave morphology were phenotyped as non-affected. Other individuals were classified as having uncertain phenotype with regard to LQTS.
For the purpose of LQTS diagnosis, we used a stationary bike (ergometer) exercise protocol as described previously. Superior to treadmill tests, ergometer tests eliminates the upper body movement to reduce ECG artifacts. An accurate QT measurement therefore can be achieved for exercise ECG recordings. 24-h Holter ECG monitoring was performed using Lifecard CF Digital Holter Recorder (Renolds Medical). LQTS phenotyping including ECG measurement was performed by G.M.V. and R.B. prior to the genetic testing.
For the bike test, we recorded standard 12-lead ECG in a paper speed of 25 mm/sec with voltage calibrated as 1 mV = 10 mm (or 10 mm/mV) for the baseline in supine and sitting positions, and exercise (3, 6, 9, 12, 15 minutes) and recovery (1, 3, 5 and 8 minutes) stages. QT interval was measured in the lead with the longest QT interval (mostly in lead II or V5) as described previously.
Isolation of human genomic DNA
Each study participant donated 5–20 ml of blood samples, which were used for isolation of genomic DNA using the DNA Isolation Kit for Mammalian Blood (Roche Diagnostic Co.)
For the two large families with LQTS, linkage analysis with markers spanning known LQTS genes was carried out to identify the specific gene for mutational analysis. Polymorphic microsatellite markers linked to LQTS genes were selected from the ABI PRISM Linkage Mapping Set-MD10 panel for linkage analysis, including D11S4046 for KCNQ1, D7S798 for KCNH2, D3S1277 for SCN5A, D4S402 for ANKB and D21S266 for KCNE1 and KCNE2. Markers were genotyped using an ABI 3100 Genetic Analyzer with the standard protocols provided by Applied Biosystems (Foster City, CA). Genotypes were analyzed using the GeneMapper 2 Software program (Applied Biosystems, Foster City, CA).
Mutational and single-strand conformational polymorphism (SSCP) analyses
Mutational analysis was carried out using direct DNA sequence analysis. All exons and exon-intron boundaries of KCNQ1 and KCNH2 were amplified by polymerase chain reaction (PCR) using primers previously published [10–12]. PCR was performed in 10 μl of standard PCR buffer containing 1.5 mM MgCl2, 0.2 mM of each dNTP, 0.5 μM of each primer, 0.1 unit of Taq DNA polymerase, and 25 ng of DNA. The amplification program was one cycle of denaturation at 94°C for 5 min, 35 cycles of 94°C for 30 s, 62°C or other annealing temperatures for each specific pair of primers for 30 s, and 72°C for 1 min, and one 7 min extension step at 72°C. The PCR products were purified using the QIAquick Gel Extraction Kit (Qiagen Inc., Valencia, CA), and sequenced with both forward and reverse primers. DNA sequencing analysis was performed using the BigDye Terminator Cycle Sequencing v3.1 kit (Applied Biosystems, Foster City, CA).
SSCP analysis was used to determine whether a mutation co-segregated with the disease in the family and whether the mutation was present in normal controls. SSCP analysis was carried out as described previously [5, 6].
Statistical differences between groups were analyzed by Student's t tests and were considered significant when P < 0.01.
We investigated 112 families with a family history of lethal cardiac events, including LQTS, for mutations and common variants in KCNQ1 and KCNH2, the two most common potassium channel genes associated with LQTS. LQTS-associated mutations were identified in eight families. No mutation was detected in the rest of 104 families. We carried out mutational analysis in 112 families with a family history of lethal cardiac events, including LQTS. LQTS-associated mutations were identified in eight families. No mutation was detected in the rest of 104 families. The results are described below.
Identification of two co-segregating variants, K897T and A490T of KCNH2 associated with LQTS in a mid-size family
Clinical characteristics of mutation carriers with KCNH2 A490T/K897T in family QW2648
Average HR (beats/min)
Low HR (beats/min)
Bradycardia (runs/24 h × beats/min)
High QTc (s)
Low QTc (s)
QTc exercise (s)
27 × 34
32 × 34
Identification of a novel KCNQ1 mutation, L187P, in a large family
DNA samples for forty-two family members from this large Utah family were available for genetic analysis. Linkage analysis with five markers for known LQTS genes revealed that the large Utah family was linked to D11S4046 at LQT1 on chromosome 11p15.5. The LOD score reached 6.11 at a recombination fraction of 0, which strongly suggests that the disease-causing gene in the family is KCNQ1. DNA sequence analysis of the DNA from the proband revealed a heterozygous T→C transition at nucleotide 560 of KCNQ1, which results in a substitution of amino acid residue leucine by proline (L187P) (Fig. 2B). The L187P mutation is located between domains S2 and S3 of KCNQ1.
To verify that the L187P mutation causes LQTS, SSCP analysis was carried out for the 42 family members with DNA samples. As shown in Fig. 1C, all affected members in the family carried the heterozygous mutation as demonstrated by the presence of two bands, whereas the normal family members showed one band, the wild type allele (Fig. 2C). The mutant SSCP band was not identified in 200 normal control individuals. These results suggest that the L187P mutation of KCNQ1 is a pathogenic mutation that causes LQTS in the family.
Identification of a novel 2-bp insertion mutation, 2020insAG in KCNH2
Identification of five other mutations in KCNH2
DNA sequence analysis of the rest of families and patients identified five previously-known mutations in the KCNH2 gene. These mutations include A561T, D609N, A614V, N629S and R366X http://www.ssi.dk/graphics/html/lqtsdb/herg.htm. Patients with mutations A561T, D609N, A614V, N629S all had a typical diagnosis of LQTS. Interestingly, the LQTS patient with mutation R366X also presented with bradycardia at the age of 30 years, torsade de pointes, recurrent syncopal episodes when awakening, startling and sitting, and first degree AV block.
In the present study, we carried out mutational analysis of KCNQ1 and KCNH2, the two most common potassium channel genes associated with LQTS in 112 families and patients with a family history of lethal cardiac events, including LQTS, Mutations were identified in 8 of 112 families. Interestingly, genotype-phenotype correlation studies in family QW2648 showed that two variants in KCNH2, mutation A490T and SNP K897T, interact with each other in cis to reduce the risk of LQTS (shorter QTc, less severe symptoms). As shown in Fig. 1, in LQTS family QW2648, two variants in the KCNH2 gene, one common SNP K897T and one mutation A490T, were identified. Because both variants co-segregated or in linkage disequilibrium in the family, they are located in the cis orientation on the same chromosome. A490T was previously reported as a de novo mutation in a Japanese female who showed markedly prolonged QTc of 0.61 s, bradycardia, torsades de pointes and recurrent syncope. Functional studies revealed that the mutant channel showed reduced current density by 39% compared to the wild type channel . In a sharp contrast, none of the seven mutation carriers with A490T and K897T showed a QTc of > 0.48 s. The difference in QTc between A490T alone and combination of both A490T and K897T was notable (Fig. 3D). These results suggest that the T allele of SNP K897T confers a protective effect against QTc prolongation. On the other hand, SNP K897T did not appear to exert any effect on bradycardia because both A490T and A490T/K897T carriers exhibited clear evidence of the bradycardia phenotype. A mutation that changes A490 to P490 was recently reported in a large family with nine LQTS patients by Pellegrino et al . The penetrance of mutation A490P was 100% in the family and the phenotype of LQTS in the family appears to be very severe. QTc ranged from 0.48 s to 0.57 s (mean QTc = 0.510 +/- 0.036), and five of the nine patients showed QTc of >0.50 s. Recurrent syncope, torsade de pointes, ventricular fibrillation, cardiac arrest, and family history of sudden death were documented in the family. The mean QTc between carriers with mutation A490P in comparison and those with both A490T and K897T was statistically significant (P = 0.0008, Fig. 3D). Our study is the first family-based genetic investigation to show that two variants in KCNH2, mutation A490T and SNP K897T, interact with each other in cis orientation and resulted in a mild LQTS phenotype.
Interestingly, no bradycardia was reported for mutations carriers with A490P, suggesting that the effect of mutation A490T on bradycardia may be mutation-specific. The molecular mechanism for mutation-specific development of bradycardia is unknown, but it is an interesting subject that warrants future investigation.
The modifying effect of KCNH2 SNP K897T has been studied previously, but inconsistency exists among different studies, mostly population-based studies. In this study, we investigated the effect of SNP K897T on QTc prolongation in multiple LQTS patients in a moderate-size family. This family-based approach has the advantage that the influence by environmental factors is more limited than a population-based approach. As described above, our results indicated that the rare T allele of SNP K897T has a protective effect against QTc prolongation (Fig. 3D). This is consistent with the results from a recent population-based study in 2,515 men and women involved in the Framingham Heart Study. In September, 2007, Newton-Cheh et al. showed that the common K allele of SNP K897T was associated with a 1.6 ms increase of QTc per allele copy , although the effect was very mild. Similarly, in 2005 in a population of 3,966 involved in the German KORA S4 study, Pfeufer et al. found that the rare T allele was associated with 1.9 ms and 3.5 ms decreases of QTc in heterozygotes and homozygotes, respectively . In 2005, Gouas et al. studied a French population with 200 subjects with short QTc (100 men with QTc of 0.333–0.363 s and 100 women with QTc of 0.336–0.365 s) and 198 subjects with longer QTc (99 men with QTc of 0.394–0.433 s and 99 women with QTc of 0.400–0.432 s) . The rare T allele was significantly more frequent in the group with short QTc than the group with long QTc (odds ratio = 0.64, P = 0.006), suggesting that the T allele was associated with shorter QTc. In 2003, Bezzina et al. found that TT homozygotes had shorter QTc than heterozygotes and KK homozygotes in a Caucasian population of 1,030 from Netherlands . The association of SNP K897T with shorter QTc was not without controversy. In 2002, Pietila et al studied 267 women and 259 men from Finland and found that the rare T allele (KT + TT) was significantly associated with longer maximum QTc than the K allele (KK) in females only (0.441 s vs. 0.477 s, P = 0.005) . In males, maximum QTc was longer in the KK group than the KT + TT group (0.465 s vs. 0.447 s), though the difference was not statistically significant (the small sample size may account for the finding of non-significance). In an Italian family Crotti et al. studied a small LQT2 family and reported a KCNH2 mutation (A1116V) and the T allele of SNP K897T on the non-mutant allele (i.e. in trans orientation) in one severe, symptomatic LQTS patient, whereas 3 relatives with A1116V alone were asymptomatic and showed mild QTc prolongation . Thus, the T allele was associated with increased QTc in the Italian family, which is contrary to the results from our study. The cis-localization between the mutation A490T and SNP K897T in our family vs. trans-localization in the study by Crotti et al. may be one of the potential causes for the discrepancy. Overall, our results are more consistent with the finding that the minor allele T of SNP K897T plays a protective role on QTc lengthening.
There are some limitations for this study. First, the comparison of the mean QTc among carriers with A490T, A490P, and A490T/K897T was made in individuals of different geographical origins under different clinical settings. The accuracy of the analysis might be compromised as the ethnic and environmental influences have not been accounted for. Furthermore, the studied family was small. Second, no modifying variants in SCN5A, KCNE1, and KCNE2 were identified in the carriers with A490T/K897T in family QW2648, however, we cannot exclude the presence of variants in other ion channels that may influence QTc and other QTc-modifiers such as NOSAP1 variants . Third, an in vitro functional study to examine the electrophysiological effects of the mutations or combinations of mutations may provide an insight into the molecular mechanism underlying the pathogenesis of LQTS.
In this study, we also identified two new mutations associated with LQTS, L187P in KCNQ1 and a KCNH2 mutation, the 2-bp insertion 2020insAG. The L187P mutation is located in the cytoplasmic loop between transmembrane domains S2 and S3 of the KCNQ1 channel. Two other mutations in the same area, G189R and R190Q, were loss-of-function mutations when expressed in Xenopus oocytes  Thus, the L187P mutation may also act by a loss-of-function mechanism. However, the mild phenotype of this large LQT1 family with 58% presented with a normal to borderline QT prolongation and only 16% of gene careers had a history of cardiac events, indicating that the functional outcome of L187P may be more complicated than a simple loss-of-function mechanism. The 2-bp insertion 2020insAG occurs at codon 674 and results in frameshift that leads to premature termination of translation. The mutant protein contains amino acid residues 1 to 673 of KCNH2 and addition of a short peptide, YQTHRCCGCGSSSASTRSPIPCASASRSTSSTPGPTPTASX. Alternatively, the frameshift creates an internal stop codon that leads to degradation of KCNH2 mutant mRNA by non-sense-mediated mRNA decay (NMD). A recent investigation that the NMD effect resulted in a mild phenotype in a large LQT2 family . However, since >30% of KCNH2 mutations are nonsense mutations that may lead to NMD, a mutation that can trigger NMD effect may not necessarily lead to a mild LQTS phenotype. The investigation of modifier effects has opened a new chapter for us to better understand why some LQTS patients die suddenly and others do not. Genotype-phenotype correlation and further molecular electrophysiology investigation may help the risk stratification.
In summary, our study identified two novel mutations causing LQTS, the L187P mutation in KCNQ1 and the 2020insAG mutation in KCNH2. Most interestingly, we showed that the rare T allele of SNP K897T conferred a protective effect on LQTS patients with KCNH2 mutation A490T located in cis orientation. Our study is the first to investigate the effect of SNP K897T on another KCNH2 mutation located in cis orientation. Together, our results expand the mutational and clinical spectrum of LQTS and provide insights into the factors that determine QT prolongation associated with increased risk of VT and sudden death.
We are grateful to the family members for their enthusiastic participation in this study. This work was supported by a China National 973 Program grant, No. 2007CB512000 and No. 2007CB512002 and an NIH/NHLBI grant, R01 HL66251 (to Q.K.W.), and Deseret Foundation Grant DF 400 (G.M.V.) and DF464 (L.Z.). Q.K.W. is an Established Investigator of the American Heart Association (0440157N).
- Roden DM, Lazzara R, Rosen M, Schwartz PJ, Towbin J, Vincent GM: Multiple mechanisms in the long-QT syndrome. Current knowledge, gaps, and future directions The SADS Foundation Task Force on LQTS. Circulation. 1996, 94: 1996-2012.View ArticlePubMedGoogle Scholar
- Chen S, Zhang L, Bryant RM, Vincent GM, Flippin M, Lee JC, Brown E, Zimmerman F, Rozich R, Szafranski P, Oberti C, Sterba R, Marangi D, Tchou PJ, Chung MK, Wang Q: KCNQ1 mutations in patients with a family history of lethal cardiac arrhythmias and sudden death. Clin Genet. 2003, 63: 273-282. 10.1034/j.1399-0004.2003.00048.x.View ArticlePubMedPubMed CentralGoogle Scholar
- Zhang L, Vincent GM, Baralle M, Baralle FE, Anson B, Benson DW, Whiting B, Timothy KW, Carlquist J, January CT, Keating MT, Splawski I: An Intronic Mutation Causes Long QT Syndrome. J Am Coll Cardiol. 2004, 44: 1283-1291. 10.1016/j.jacc.2004.06.045.View ArticlePubMedGoogle Scholar
- Zhang L, Timothy KW, Vincent GM, et al: The spectrum of ST-T wave patterns and repolarization parameters in congenital long QT syndrome: ECG findings identify genotype. Circulation. 2000, 102: 2849-2855.View ArticlePubMedGoogle Scholar
- Wang Q, Curren ME, Splawski I, Burn TC, Millholland JM, VanRaay TJ, Shen J, Timothy KW, Vincent GM, de Jager T, Schwartz PJ, Towbin JA, Moss AJ, Atkinson DL, Landes GM, Connors TD, Keating MT: Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias. Nature Genet. 1996, 12: 17-23. 10.1038/ng0196-17.View ArticlePubMedGoogle Scholar
- Wang Q, Shen J, Splawski I, Atkinson D, Li Z, Robinson JL, Moss AJ, Towbin JA, Keating MT: SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome. Cell. 1995, 80: 805-811. 10.1016/0092-8674(95)90359-3.View ArticlePubMedGoogle Scholar
- Tanaka T, Nagai R, Tomoike H, Takata S, Yano K, Yabuta K, Haneda N, Nakano O, Shibata A, Sawayama T, Kasai H, Yazaki Y, Nakamura Y: Four novel KVLQT1 and four novel HERG mutations in familial long-QT syndrome. Circulation. 1997, 95: 565-567.View ArticlePubMedGoogle Scholar
- Vincent GM, Timothy KW, Leppert M, et al: The spectrum of symptoms and QT Intervals in the carriers of the gene for the long-QT syndrome. N Engl J Med. 1992, 327: 846-852.View ArticlePubMedGoogle Scholar
- Vincent GM, Jaiswal D, Timothy KW: Effects of exercise on heart rate, QT, QTc and QT/QS2 in the Romano-Ward inherited long QT syndrome. Am J Cardiol. 1991, 68: 498-503. 10.1016/0002-9149(91)90785-J.View ArticlePubMedGoogle Scholar
- Wang Q, Curran ME, Splawski I, Burn TC, Millholland JM, VanRaay TJ, Shen J, Timothy KW, Vincent GM, de Jager T, Schwartz PJ, Toubin JA, Moss AJ, Atkinson DL, Landes GM, Connors TD, Keating MT: Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias. Nat Genet. 1996, 12: 17-23. 10.1038/ng0196-17.View ArticlePubMedGoogle Scholar
- Curran ME, Splawski I, Timothy KW, Vincent GM, Green ED, Keating MT: A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome. Cell. 1995, 80: 795-803. 10.1016/0092-8674(95)90358-5.View ArticlePubMedGoogle Scholar
- Westenskow P, Splawski I, Timothy KW, Keating MT, Sanguinetti MC: Compound mutations: a common cause of severe long-QT syndrome. Circulation. 2004, 109: 1834-1841. 10.1161/01.CIR.0000125524.34234.13.View ArticlePubMedGoogle Scholar
- Yoshida H, Horie M, Otani H, Kawashima T, Onishi Y, Sasayama S: Bradycardia-induced long QT syndrome caused by a de novo missense mutation in the S2-S3 inner loop of HERG. Am J Med Genet. 2001, 98: 348-352. 10.1002/1096-8628(20010201)98:4<348::AID-AJMG1109>3.0.CO;2-A.View ArticlePubMedGoogle Scholar
- Pellegrino PL, Bafunno V, Ieva R, Brunetti ND, Mavilio G, Sessa F, Grimaldi M, Margaglione M, Di Biase M: A novel mutation in human ether-a-go-go- related gene, alanine to proline at position 490, found in a large family with autosomal dominant long QT syndrome. Am J Cardiol. 2007, 99: 1737-1740. 10.1016/j.amjcard.2007.01.056.View ArticlePubMedGoogle Scholar
- Newton-Cheh C, Guo CY, Larson MG, Musone SL, Surti A, Camargo AL, Drake JA, Benjamin EJ, Levy D, D'Agostino RB, Hirschhorn JN, O'donnell CJ: Common Genetic Variation in KCNH2 Is Associated With QT Interval Duration: The Framingham Heart Study. Circulation. 2007, 116: 1128-1136. 10.1161/CIRCULATIONAHA.107.710780.View ArticlePubMedGoogle Scholar
- Pfeufer A, Jalilzadeh S, Perz S, Mueller JC, Hinterseer M, Illig T, Akyol M, Huth C, Schopfer-Wendels A, Kuch B, Steinbeck G, Holle R, Nabauer M, Wichmann HE, Meitinger T, Kaab S: Common variants in myocardial ion channel genes modify the QT interval in the general population:results from the KORA study. Circ Res. 2005, 96: 693-697. 10.1161/01.RES.0000161077.53751.e6.View ArticlePubMedGoogle Scholar
- Gouas L, Nicaud V, Berthet M, Forhan A, Tiret L, Balkau B, Guicheney P: Association of KCNQ1, KCNE1, KCNH2 and SCN5A polymorphisms with QTc interval length in a healthy population. Eur J Hum Genet. 2005, 13: 1213-1222. 10.1038/sj.ejhg.5201489.View ArticlePubMedGoogle Scholar
- Bezzina CR, Verkerk AO, Busjahn A, Jeron A, Erdmann J, Koopmann TT, Bhuiyan ZA, Wilders R, Mannens MM, Tan HL, Luft FC, Schunkert H, Wilde AA: A common polymorphism in KCNH2 (HERG) hastens cardiac Repolarization. Cardiovasc Res. 2003, 59: 27-36. 10.1016/S0008-6363(03)00342-0.View ArticlePubMedGoogle Scholar
- Pietila E, Fodstad H, Niskasaari E, Laitinen PP, Swan H, Savolainen M, Kesaniemi YA, Kontula K, Huikuri HV: Association between HERG K897T polymorphism and QT interval in middle-aged Finnish women. J Am Coll Cardiol. 2002, 40: 511-514. 10.1016/S0735-1097(02)01979-4.View ArticlePubMedGoogle Scholar
- Crotti L, Lundquist AL, Insolia R, Pedrazzini M, Ferrandi C, De Ferrari GM, Vicentini A, Yang P, Roden DM, George AL, Schwartz PJ: KCNH2-K897T is a genetic modifier of latent congenital long-QT syndrome. Circulation. 2005, 112: 1251-1258. 10.1161/CIRCULATIONAHA.105.549071.View ArticlePubMedGoogle Scholar
- Arking DE, Pfeufer A, Post W, Kao WH, Newton-Cheh C, Ikeda M, West K, Kashuk C, Akyol M, Perz S, Jalilzadeh S, Illig T, Gieger C, Guo CY, Larson MG, Wichmann HE, Marbán E, O'Donnell CJ, Hirschhorn JN, Kääb S, Spooner PM, Meitinger T, Chakravarti A: A common genetic variant in the NOS1 regulator NOS1AP modulates cardiac repolarization. Nat Genet. 2006, 38: 644-651. 10.1038/ng1790.View ArticlePubMedGoogle Scholar
- Wang Z, Tristani-Firouzi M, Xu Q, Lin M, Keating MT: Sanguinetti MC.Functional effects of mutations in KvLQT1 that cause long QT syndrome. J Cardiovasc Electrophysiol. 1999, 10: 817-826. 10.1111/j.1540-8167.1999.tb00262.x.View ArticlePubMedGoogle Scholar
- Gong Q, Zhang L, Vincent GM, Horne BD, Zhou ZF: Nonsense Mutations in hERG Cause a Decrease in Mutant mRNA Transcripts by Nonsense-mediated mRNA Decay in Human Long QT Syndrome. Circulation. 2007, 116: 17-24. 10.1161/CIRCULATIONAHA.107.708818.View ArticlePubMedPubMed CentralGoogle Scholar
- The pre-publication history for this paper can be accessed here:http://0-www.biomedcentral.com.brum.beds.ac.uk/1471-2350/9/87/prepub
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