CORC

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Whole Exome Sequencing Identified a Pathogenic Mutation in RYR2 in a Chinese Family with Unexplained Sudden Death (CPCI-S收录) 会议
作者:  Lin, Yubi[1,2,3,4,5,6];  Liao, Zili[1,2,3,4,5];  He, Siqi[1,2,3,4,5,6];  Liu, Ruilin[7];  Peng, Yongzheng[8]
收藏  |  浏览/下载:2/0  |  提交时间:2019/04/11
SCN5A Mutants Associated with Familial Cardiac Sodium Overlap Syndrome Characterized as Sick Sinus Syndrome, Atrial Fibrillation, Brugada Syn (CPCI-S收录) 会议
作者:  Lin, Yubi[1,2];  Deng, Chunyu[1,2];  Zhan, XianZhang[1,2];  Xu, Zhe[3];  Zhu, Jiening[1,2]
收藏  |  浏览/下载:11/0  |  提交时间:2019/04/11


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