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CEP78 is mutated in a distinct type of Usher syndrome 期刊论文
JOURNAL OF MEDICAL GENETICS, 2017, 卷号: 54, 期号: 3
作者:  Fu, Qing;  Xu, Mingchu;  Chen, Xue;  Sheng, Xunlun;  Yuan, Zhisheng
收藏  |  浏览/下载:8/0  |  提交时间:2019/12/05
Brain Network for the Core Deficits of Semantic Dementia: A Neural Network Connectivity-Behavior Mapping Study 期刊论文
FRONTIERS IN HUMAN NEUROSCIENCE, 2017, 卷号: 11
作者:  Chen, Yan;  Chen, Keliang;  Ding, Junhua;  Zhang, Yumei;  Yang, Qing
收藏  |  浏览/下载:10/0  |  提交时间:2019/12/05
The phenotypic variability of HK1-associated retinal dystrophy 期刊论文
SCIENTIFIC REPORTS, 2017, 卷号: 7
作者:  Yuan, Zhisheng;  Li, Baiyu;  Xu, Mingchu;  Chang, Emmanuel Y.;  Li, Huajin
收藏  |  浏览/下载:5/0  |  提交时间:2019/12/05


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