Open AccessWhole-Exome Sequencing Identified a Novel Desmoglein-2 Gene Mutation Associated with Familial Arrhythmogenic Right Ventricular Cardiomyopathy
Author(s) -
Nianwei Zhou,
Yili Liu,
Shengmei Qin,
Weipeng Zhao,
Lu Tang,
Cuizhen Pan,
Zilong Qiu,
Xiaolin Wang,
Xianhong Shu
Publication year - 2017
Publication title -
cardiology plus
Language(s) - English
Resource type - Journals
eISSN - 2470-752X
pISSN - 2470-7511
DOI - 10.4103/2470-7511.248376
Subject(s) - sanger sequencing , exome sequencing , proband , genetics , exome , mutation , dna sequencing , exon , medicine , biology , gene
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