Human Genome Epidemiology Literature Finder
Records 1 - 2 (of 2 Records) |
Query Trace: Epilepsy and NIPA2[original query] |
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NIPA2 located in 15q11.2 is mutated in patients with childhood absence epilepsy. Human genetics 2012 Jul 131 (7): 1217-24. Jiang Yuwu, Zhang Yuehua, Zhang Pingping, Sang Tian, Zhang Feng, Ji Taoyun, Huang Qionghui, Xie Han, Du Renqian, Cai Bin, Zhao Haijuan, Wang Jingmin, Wu Ye, Wu Husheng, Xu Keming, Liu Xiaoyan, Chan Piu, Wu Xi |
Genetic counseling for susceptibility loci and neurodevelopmental disorders: the del15q11.2 as an example. American journal of medical genetics. Part A 2013 Nov 161A (11): 2846-54. De Wolf Veerle, Brison Nathalie, Devriendt Koenraad, Peeters Hil |
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