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The CNTN4 c.4256C>T mutation is rare in Japanese with inherited spinocerebellar ataxia
Eiji Tanaka, Hirofumi Maruyama, Hiroyuki Morino, Eiko Nakajima, Hideshi KawakamiVolume:
266
Year:
2008
Language:
english
DOI:
10.1016/j.jns.2007.09.004
File:
PDF, 84 KB
english, 2008