Human Genome Epidemiology Literature Finder

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Query Trace: Ataxia and CNTN4[original query]
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 Similar articles in PubMed