CORC

浏览/检索结果: 共5条,第1-5条 帮助

已选(0)清除 条数/页:   排序方式:
Case report of familial sudden cardiac death caused by a DSG2 p.F531C mutation as genetic background when carrying with heterozygous KCNE5 p.D92E/E93X mutation 期刊论文
2018, 卷号: 19
作者:  Lin, Yubi[1,2];  Huang, Jiana[1,3];  He, Siqi[1,3];  Feng, Ruiling[1,3];  Zhong, ZhiAn[2]
收藏  |  浏览/下载:6/0  |  提交时间:2019/12/17
Whole Genome Sequence Identified a Rare Homozygous Pathogenic Mutation of the DSG2 Gene in a Familial Arrhythmogenic Cardiomyopathy Involving Both Ventricles 期刊论文
2017, 卷号: 138, 期号: 1, 页码: 41
作者:  Lin, Yubi[1,2];  Zhang, Qianhuan[1];  Zhong, Zhi An[1];  Xu, Zhe[3];  He, Siqi[1,2]
收藏  |  浏览/下载:17/0  |  提交时间:2019/12/06
Familial Sudden Cardiac Death Caused by DSG2 Mutation as Genetic Backgrounds: Whole Exome Sequencing and Valid Therapy of Catheter Ablation (CPCI-S收录) 会议
作者:  Lin, Yubi[1,2,3,4,5,6,7];  Zhang, Qianhuan[1,2,3,4,5,6];  Chen, Jia[8];  Feng, Ruiling[1,2,3,4,5,6,7];  He, Siqi[1,2,3,4,5,6,7]
收藏  |  浏览/下载:8/0  |  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
SCN5A Mutants Associated with Familial Cardiac Sodium Overlap Syndrome Characterized as Sick Sinus Syndrome, Atrial Fibrillation, Brugada Syndrome, and Progressive Conduction Disease 会议论文
Beijing, PEOPLES R CHINA, OCT 12-15, 2017
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:13/0  |  提交时间:2019/12/10


©版权所有 ©2017 CSpace - Powered by CSpace