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A genome-wide association study in Han Chinese identifies a susceptibility locus for primary Sjogren's syndrome at 7q11.23 期刊论文
NATURE GENETICS, 2013, 卷号: 45, 期号: 11, 页码: 1361-+
作者:  Li, YZ;  Zhang, KL;  Chen, H;  Sun, F;  Xu, JJ
收藏  |  浏览/下载:5/0  |  提交时间:2016/03/29
A Novel Mutation Impairing the Tertiary Structure and Stability of gamma C-Crystallin (CRYGC) Leads to Cataract Formation in Humans and Zebrafish Lens 期刊论文
HUMAN MUTATION, 2012, 卷号: 33, 期号: 2, 页码: 391-401
作者:  Li, XQ;  Cai, HC;  Zhou, SY;  Yang, JH;  Xi, YB
收藏  |  浏览/下载:2/0  |  提交时间:2015/12/14
A Novel CRYGD Mutation (p.Trp43Arg) Causing Autosomal Dominant Congenital Cataract in a Chinese Family 期刊论文
HUMAN MUTATION, 2011, 卷号: 32, 期号: 1, 页码: E1939-E1947
作者:  Wang, BB;  Yu, CH;  Xi, YB;  Cai, HC;  Wang, J
收藏  |  浏览/下载:4/0  |  提交时间:2015/12/14


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