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

<div>Schematic of the transmembrane topology of the<i> SCN5A</i> protein. The location of the variants R34H (c.101G&gt;A) and V1278I (c.3832G&gt;A) is shown.</div>

Disease Markers

fig5

Figure 5

Figure 5: Exome Sequencing Identifies Compound Heterozygous Mutations in<i> SCN5A</i> Associated with Congenital Complete Heart Block in the Thai Population 

Figure 5 | Exome Sequencing Identifies Compound Heterozygous Mutations in SCN5A Associated with Congenital Complete Heart Block in the Thai Population 