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Novel SEA and LG2 Agrin mutations causing congenital Myasthenic syndrome 期刊论文
ORPHANET JOURNAL OF RARE DISEASES, 2017, 卷号: 12
作者:  Zhao, Chongbo;  Xi, Jianying
收藏  |  浏览/下载:9/0  |  提交时间:2019/12/05
Disrupted-in-Schizophrenia-1 (DISC1) protein disturbs neural function in multiple disease-risk pathways 期刊论文
HUMAN MOLECULAR GENETICS, 2017, 卷号: 26, 期号: 14, 页码: 2634-2648
作者:  Shao, Lisha;  Lu, Binyan;  Wen, Zhexing;  Teng, Shaolei;  Wang, Lingling
收藏  |  浏览/下载:3/0  |  提交时间:2022/03/28


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