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Reduced Penetrance of PRRT2 Mutation in a Chinese Family With Infantile Convulsion and Choreoathetosis Syndrome 期刊论文
JOURNAL OF CHILD NEUROLOGY, 2015, 卷号: 30, 期号: 10
作者:  Zhang, L. M.;  An, Y.;  Pan, G.;  Ding, Y. F.;  Zhou, Y. F.
收藏  |  浏览/下载:6/0  |  提交时间:2019/12/19
Re-evaluation of PRRT2 mutations in paroxysmal disorders 期刊论文
2014, 卷号: 261, 期号: 5, 页码: 951-953
作者:  Guo, Xia Nan;  Lu, Qiang;  Zhou, Xiang Qin;  Liu, Qing;  Zhang, Xue
收藏  |  浏览/下载:3/0  |  提交时间:2020/01/13
PRRT2 c.649dupC Mutation Derived from De Novo in Paroxysmal Kinesigenic Dyskinesia 期刊论文
CNS NEUROSCIENCE & THERAPEUTICS, 2013, 卷号: 19, 期号: 1, 页码: 61-65
Li, HF; Ni, W; Xiong, ZQ; Xu, JF; Wu, ZY
收藏  |  浏览/下载:65/0  |  提交时间:2013/06/04


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