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

<div>Filtering procedure of variants obtained by whole exome sequencing 2nd data analysis.</div>

Disease Markers

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Figure 3

Figure 3: Exome Sequencing Identifies Compound Heterozygous Mutations in<i> SCN5A</i> Associated with Congenital Complete Heart Block in the Thai Population 

Figure 3 | Exome Sequencing Identifies Compound Heterozygous Mutations in SCN5A Associated with Congenital Complete Heart Block in the Thai Population 