Exome Sequencing Identifies Compound Heterozygous Mutations in SCN5A Associated with Congenital Complete Heart Block in the Thai Population

Figure 4

Chromatograms of 2 heterozygous missense variants in SCN5A gene: c.101G>A (a) and c.3832G>A (b). Letters in indicate complementary (FWD) alleles.

(a) SCN5A  c.101G>A [C>T]

(b) SCN5A  c.3832G>A [C>T]