机构：[1]Department of Pediatrics, Peking University First Hospital, Beijing 100034, China[2]School of Life Sciences, Fudan University, Shanghai, China[3]Department of Neurobiology and Neurology, Xuanwu Hospital of Capital Medical University, #45 Changchun Street, Beijing 100053, China神经内科首都医科大学宣武医院
Acknowledgments We very appreciate our patients and their families for their cooperation. this report was supported by the Ministry of Science and technology of China (grants: 2006AA02A408, 2006CB500701, 2008ZX09312-014, 2011CBA00401).
第一作者机构：[1]Department of Pediatrics, Peking University First Hospital, Beijing 100034, China
通讯作者：
通讯机构：[1]Department of Pediatrics, Peking University First Hospital, Beijing 100034, China[3]Department of Neurobiology and Neurology, Xuanwu Hospital of Capital Medical University, #45 Changchun Street, Beijing 100053, China
推荐引用方式(GB/T 7714)：
Yuwu Jiang,Yuehua Zhang,Pingping Zhang,et al.NIPA2 mutations are correlative with childhood absence epilepsy in the Han Chinese population[J].HUMAN GENETICS.2014,133(5):675-676.doi:10.1007/s00439-014-1428-2.
APA：
Yuwu Jiang,Yuehua Zhang,Pingping Zhang,Feng Zhang,Han Xie...&Xiru Wu.(2014).NIPA2 mutations are correlative with childhood absence epilepsy in the Han Chinese population.HUMAN GENETICS,133,(5)
MLA：
Yuwu Jiang,et al."NIPA2 mutations are correlative with childhood absence epilepsy in the Han Chinese population".HUMAN GENETICS 133..5(2014):675-676
