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[A pedigree of Charcot-Marie-Tooth disease type 4F (Periaxin mutation)].
Shimohata M, Hirahara K, Igarashi S, Hara K, Kijima K, Onodera O, Tanaka K, Nishizawa M, Tsuji S, Hayasaka K. Shimohata M, et al. Among authors: hara k. Rinsho Shinkeigaku. 2005 Mar;45(3):221-5. Rinsho Shinkeigaku. 2005. PMID: 15835292 Review. Japanese.
Spinocerebellar ataxia type 15.
Gardner RJ, Knight MA, Hara K, Tsuji S, Forrest SM, Storey E. Gardner RJ, et al. Among authors: hara k. Cerebellum. 2005;4(1):47-50. doi: 10.1080/14734220410019029. Cerebellum. 2005. PMID: 15895559 Review.
4,218 results