Whole-exome sequencing identified a novel desmoglein-2 gene mutation associated with familial arrhythmogenic right ventricular cardiomyopathy

Whole-exome sequencing identified a novel desmoglein-2 gene mutation associated with familial arrhythmogenic right ventricular cardiomyopathy

Objective: The objective of this study is to evaluate novel variations in a Chinese family of Han ethnicity, with arrhythmogenic right ventricular cardiomyopathy (ARVC) by the powerful technology of whole-exome sequencing (WES). Methods: Genomic DNA from representative family members was extracted a...

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Bibliographic Details
Main Authors: Nianwei Zhou, Yili Liu, Shengmei Qin, Weipeng Zhao, Lu Tang, Cuizhen Pan, Zilong Qiu, Xiaolin Wang, Xianhong Shu
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2017-01-01
Series:Cardiology Plus
Subjects:
Arrhythmogenic right ventricular cardiomyopathy
desmoglein-2
whole-exome sequencing
Online Access:http://www.cardiologyplus.org/article.asp?issn=2470-7511;year=2017;volume=2;issue=3;spage=8;epage=12;aulast=Zhou

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