Skip to main content
Fig. 3 | BMC Medical Genetics

Fig. 3

From: SLC4A4 compound heterozygous mutations in exon–intron boundary regions presenting with severe proximal renal tubular acidosis and extrarenal symptoms coexisting with Turner’s syndrome: a case report

Fig. 3

Identification of fragments of SLC4A4 coding sequences (a) and β-actin (as a control; b) in cDNA of the proband and control healthy human. Reverse-transcription PCR (RT-PCR) products of the SLC4A4 coding region were not detected in the proband. In contrast, the fragment of β-actin was detected in the proband’s cDNA. PT, proband; P/C, positive control (the cDNA from white blood cells of a healthy human as a template); N/C, negative control (no template). c quantitative RT-PCR (qRT-PCR) in cDNA provided by the proband, parents and control. n = 2 each. ***: p < 0.01, **: P < 0.05, *: P < 0.1

Back to article page

BMC Medical Genetics

ISSN: 1471-2350

Contact us