Exome sequencing identifies truncating mutations in PRRT2 that cause paroxysmal kinesigenic dyskinesia

Wan‐Jin Chen; Yu Lin; Zhi‐Qi Xiong; Wei Wei; Ni Wang; Guohe Tan; Shunling Guo; J. He; Ya‐Fang Chen; Qi‐Jie Zhang; Hong‐Fu Li; Yi Lin; Shen-Xing Murong; Jianfeng Xu; Ning Wang; Zhi‐Ying Wu

doi:10.1038/ng.1008

Exome sequencing identifies truncating mutations in PRRT2 that cause paroxysmal kinesigenic dyskinesia

Wan‐Jin Chen(Fudan University), Yu Lin(First Affiliated Hospital of Fujian Medical University), Zhi‐Qi Xiong(Chinese Academy of Sciences), Wei Wei(First Affiliated Hospital of Fujian Medical University), Ni Wang(First Affiliated Hospital of Fujian Medical University), Guohe Tan(Shanghai Institutes for Biological Sciences), Shunling Guo(Shanghai Institutes for Biological Sciences), J. He(Fujian Medical University), Ya‐Fang Chen(Fujian Medical University), Qi‐Jie Zhang(Fujian Medical University), Hong‐Fu Li(State Key Laboratory of Medical Neurobiology), Yi Lin(Fujian Medical University), Shen-Xing Murong(First Affiliated Hospital of Fujian Medical University), Jianfeng Xu(Huashan Hospital), Ning Wang(Fujian Medical University), Zhi‐Ying Wu(Huashan Hospital)

Nature Genetics

November 20, 2011

10.1038/ng.1008

Cited by 484

Abstract

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