Genetic spectrum of Charcot-Marie-Tooth disease associated with myelin protein zero gene variants in Japan

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作者： Taniguchi, Takaki ^[1] ; Ando, Masahiro ^[2] ; Okamoto, Yuji ^[3] ; Yoshimura, Akiko ^[4] ; Higuchi, Yujiro ^[5] ; Hashiguchi, Akihiro ; Shiga, Kensuke ; Hayashida, Arisa ; Hatano, Taku ; Ishiura, Hiroyuki ; Mitsui, Jun ; Hattori, Nobutaka ; Mizuno, Toshiki ; Nakagawa, Masanori ; Tsuji, Shoji ; Takashima, Hiroshi

作者单位： Kagoshima Univ, Grad Sch Med & Dent Sci, Dept Neurol & Geriatr, Kagoshima, Japan ^[1] Matsushita Mem Hosp, Dept Neurol, Osaka, Japan ^[2] Kyoto Prefectural Univ Med, Dept Neurol, Kyoto, Japan ^[3] Univ Tokyo, Grad Sch Med, Dept Mol Neurol, Tokyo, Japan ^[4] Juntendo Univ, Sch Med, Dept Neurol, Tokyo, Japan ^[5]

关键词 cerebrospinal fluid protein Charcot&8211 Marie&Tooth disease cranial nerve involvement creatine kinase myelin P0 protein

发布时间 2021-05-08

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