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

<div>The lineage of the family with complete heart block indicated by the dark symbol, females by circles, and males by squares. Letters (a) and (b) indicate genotypes of 2 variants in the<i> SCN5A</i> gene for c.101G&gt;A and c.3832G&gt;A. The homozygous reference genotypes are indicated by (−/−) and heterozygous alternate genotypes by (−/+). The genotypes of II-1 are presumed genotypes which are inferred from his children.</div>

Disease Markers

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Figure 2

Figure 2: Exome Sequencing Identifies Compound Heterozygous Mutations in<i> SCN5A</i> Associated with Congenital Complete Heart Block in the Thai Population 

Figure 2 | Exome Sequencing Identifies Compound Heterozygous Mutations in SCN5A Associated with Congenital Complete Heart Block in the Thai Population 