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

✍ Scribed by Chen, Wan-Jin; Lin, Yu; Xiong, Zhi-Qi; Wei, Wei; Ni, Wang; Tan, Guo-He; Guo, Shun-Ling; He, Jin; Chen, Ya-Fang; Zhang, Qi-Jie; Li, Hong-Fu; Lin, Yi; Murong, Shen-Xing; Xu, Jianfeng; Wang, Ning; Wu, Zhi-Ying

Book ID: 121478053
Publisher: Nature Publishing Group
Year: 2011
Tongue: English
Weight: 741 KB
Volume: 43
Category: Article
ISSN: 1061-4036
DOI: 10.1038/ng.1008

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