NIPA2 located in 15q11.2 is mutated in patients with childhood absence epilepsy.

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Published in Hum Genet on February 26, 2012

Authors

Yuwu Jiang1, Yuehua Zhang, Pingping Zhang, Tian Sang, Feng Zhang, Taoyun Ji, Qionghui Huang, Han Xie, Renqian Du, Bin Cai, Haijuan Zhao, Jingmin Wang, Ye Wu, Husheng Wu, Keming Xu, Xiaoyan Liu, Piu Chan, Xiru Wu

Author Affiliations

1: Department of Pediatrics, Peking University First Hospital, Beijing 100034, China. drjiangyw@gmail.com

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