Compound and heterozygous mutations of DSG2 identified by Whole Exome Sequencing in arrhythmogenic right ventricular cardiomyopathy/dysplasia with ventricular tachycardia

This study was designed to identify the pathogenic mutations in two Chinese families of arrhythmogenic right ventricular cardiomyopathy/dysplasia (ARVC/D) using the Whole Exome Sequencing (WES).

Source: Journal of Electrocardiology - June 20, 2018 Category: Cardiology Authors: Yubi Lin, Jiana Huang, Ting Zhao, Siqi He, Zifeng Huang, Xiumin Chen, Hongwen Fei, Haiying Luo, Hui Liu, Shulin Wu, Xiufang Lin Source Type: research