Discovery of Digenic Mutation, KCNH2...

Cardiovascular Innovations and Applications 2020 / 07 Vol. 4; Iss. 4

Discovery of Digenic Mutation, KCNH2 c.1898A >C and JUP c.916dupA, in a Chinese Family with Long QT Syndrome via Whole-Exome Sequencing

Zhai, Yafei, Miao, Jinxin, Peng, Ying, Fang, Guangming, Wang, Chuchu, Wang, Yaohe, Zhao, Xiaoyan, Dong, Jianzeng
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Volume:
4
Journal:
Cardiovascular Innovations and Applications
DOI:
10.15212/cvia.2019.0578
Date:
July, 2020
File:
PDF, 2.39 MB
2020
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