Whole-Exome Sequencing Identifies a Novel <i>TRPM4</i> Mutation in a Chinese Family with Atrioventricular Block

<div>Description of the family with AVB. (a) Pedigree of the family. Family members are identified by generations and numbers. Squares = males; circles = females; black symbols = affected individuals; white symbols = unaffected individuals; arrow = the proband; M/N = people carried <i>TRPM4</i> mutation; N/N = people without <i>TRPM4</i> mutation. (b) The 12-lead ECGs of the proband. (c) Sanger sequencing results of the TRPM4 mutation. Sequence chromatogram indicates a C to T transition of nucleotide 2455.</div>

BioMed Research International

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Figure 1

Figure 1: Whole-Exome Sequencing Identifies a Novel <i>TRPM4</i> Mutation in a Chinese Family with Atrioventricular Block 

BioMed Research International

Whole-Exome Sequencing Identifies a Novel TRPM4 Mutation in a Chinese Family with Atrioventricular Block

Figure 1