Exome sequencing identifies truncating mutations in PRRT2 that cause paroxysmal kinesigenic dyskinesia (Q24297970)

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Exome sequencing identifies truncating mutations in PRRT2 that cause paroxysmal kinesigenic dyskinesia
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    Exome sequencing identifies truncating mutations in PRRT2 that cause paroxysmal kinesigenic dyskinesia (English)
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    Wan-Jin Chen
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    Yu Lin
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    Zhi-Qi Xiong
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    Wei Wei
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    Wang Ni
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    Guo-He Tan
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    Shun-Ling Guo
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    Jin He
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    Ya-Fang Chen
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    Qi-Jie Zhang
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    Hong-Fu Li
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    Yi Lin
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    Shen-Xing Murong
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    Jianfeng Xu
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    Ning Wang
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    Zhi-Ying Wu
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    December 2011
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    43
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    1252-5
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    12
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