Fig. 3From: Whole exome sequencing reveals two novel compound heterozygous mutations in TWNK as a cause of the hepatocerebral form of mitochondrial DNA depletion syndrome: a case reportSequence chromatograms of this Chinese family. (a) TWNK c.1186C > T (p.Pro396Ser) from the proband (b) TWNK c.1844G > C (p.Gly615Ala) from the proband (c) TWNK c.1186C > T (p.Pro396Ser) from the father (d) TWNK c.1844G > C (p.Gly615Ala) from the motherBack to article page