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Iwabuchi K, Endoh S, Hagimoto H, Okamoto K, Miyakawa T, Yamaguchi T, Kajiwara A, Inoue K, Yamada Y, Amano N. [Three patients from two families with familial Creutzfeldt-Jakob disease having a point mutation in the prion protein gene at codon 200 (Glu-->Lys)]. No To Shinkei. 1994 Apr;46(4):349–54. PMID: 7912945. |