Compound and heterozygous mutations of KCNQ1...

Annals of Noninvasive Electrocardiology 2019 / 09

Compound and heterozygous mutations of KCNQ1 in long QT syndrome with familial history of unexplained sudden death: Identified by analysis of whole exome sequencing and predisposing genes

Lin, Yubi, Zhao, Ting, He, Siqi, Huang, Jiana, Liu, Qianru, Yang, Zhe, Qin, Jiading, Yu, Nan, Lu, Hongyun, Lin, Xiufang
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Journal:
Annals of Noninvasive Electrocardiology
DOI:
10.1111/anec.12694
Date:
September, 2019
File:
PDF, 1.90 MB
2019
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