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Genetic spectrum of Charcot-Marie-Tooth disease associated with myelin protein zero gene variants in Japan.
Taniguchi, Takaki; Ando, Masahiro; Okamoto, Yuji; Yoshimura, Akiko; Higuchi, Yujiro; Hashiguchi, Akihiro; Shiga, Kensuke; Hayashida, Arisa; Hatano, Taku; Ishiura, Hiroyuki; Mitsui, Jun; Hattori, Nobutaka; Mizuno, Toshiki; Nakagawa, Masanori; Tsuji, Shoji; Takashima, Hiroshi.
Afiliação
  • Taniguchi T; Department of Neurology and Geriatrics, Kagoshima University Graduate School of Medical and Dental Sciences, Kagoshima, Japan.
  • Ando M; Department of Neurology and Geriatrics, Kagoshima University Graduate School of Medical and Dental Sciences, Kagoshima, Japan.
  • Okamoto Y; Department of Neurology and Geriatrics, Kagoshima University Graduate School of Medical and Dental Sciences, Kagoshima, Japan.
  • Yoshimura A; Department of Physical Therapy, School of Health Sciences, Faculty of Medicine, Kagoshima University, Kagoshima, Japan.
  • Higuchi Y; Department of Neurology and Geriatrics, Kagoshima University Graduate School of Medical and Dental Sciences, Kagoshima, Japan.
  • Hashiguchi A; Department of Neurology and Geriatrics, Kagoshima University Graduate School of Medical and Dental Sciences, Kagoshima, Japan.
  • Shiga K; Department of Neurology and Geriatrics, Kagoshima University Graduate School of Medical and Dental Sciences, Kagoshima, Japan.
  • Hayashida A; Department of Neurology, Matsushita Memorial Hospital, Osaka, Japan.
  • Hatano T; Department of Neurology, Kyoto prefectural University of Medicine, Kyoto, Japan.
  • Ishiura H; Department of Neurology, Juntendo University School of Medicine, Tokyo, Japan.
  • Mitsui J; Department of Neurology, Juntendo University School of Medicine, Tokyo, Japan.
  • Hattori N; Department of Molecular Neurology, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
  • Mizuno T; Department of Molecular Neurology, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
  • Nakagawa M; Department of Neurology, Juntendo University School of Medicine, Tokyo, Japan.
  • Tsuji S; Department of Neurology, Kyoto prefectural University of Medicine, Kyoto, Japan.
  • Takashima H; Department of Neurology, Kyoto prefectural University of Medicine, Kyoto, Japan.
Clin Genet ; 99(3): 359-375, 2021 03.
Article em En | MEDLINE | ID: mdl-33179255
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Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Variação Genética / Doença de Charcot-Marie-Tooth / Proteína P0 da Mielina / Predisposição Genética para Doença / Nervos Cranianos Tipo de estudo: Observational_studies / Risk_factors_studies Limite: Adolescent / Adult / Aged / Child / Child, preschool / Female / Humans / Male / Middle aged / Newborn País/Região como assunto: Asia Idioma: En Revista: Clin Genet Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Japão
Texto completo
Adicionar na Minha BVS
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Variação Genética / Doença de Charcot-Marie-Tooth / Proteína P0 da Mielina / Predisposição Genética para Doença / Nervos Cranianos Tipo de estudo: Observational_studies / Risk_factors_studies Limite: Adolescent / Adult / Aged / Child / Child, preschool / Female / Humans / Male / Middle aged / Newborn País/Região como assunto: Asia Idioma: En Revista: Clin Genet Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Japão