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

Yafei Zhai,Jinxin Miao,Ying Peng,Guangming Fang,Chuchu Wang,Yaohe Wang,Xiaoyan Zhao,Jianzeng Dong

Cardiovascular Innovations and Applications（2020）

Cited 1|Views7
Key words
Long QT syndrome (LQTS),Digenic mutation,KCNH2,JUP
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