Human Genome Epidemiology Literature Finder
Records 1 - 2 (of 2 Records) |
Query Trace: Ataxia and SCA16[original query] |
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The CNTN4 c.4256C>T mutation is rare in Japanese with inherited spinocerebellar ataxia. Journal of the neurological sciences 2008 Mar 266 (1-2): 180-1. Tanaka Eiji, Maruyama Hirofumi, Morino Hiroyuki, Nakajima Eiko, Kawakami Hides |
Identification of a Splicing Mutation in ITPR1 via WES in a Chinese Early-Onset Spinocerebellar Ataxia Family. Cerebellum (London, England) 2017 12 17 (3): 294-299. Wang Li, Hao Ying, Yu Peng, Cao Zhenhua, Zhang Jin, Zhang Xin, Chen Yuanyuan, Zhang Hao, Gu Weiho |
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