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Genetic and functional analysis of KIF5A variants in Japanese patients with sporadic amyotrophic lateral sclerosis.
Nakamura, Ryoichi; Tohnai, Genki; Atsuta, Naoki; Nakatochi, Masahiro; Hayashi, Naoki; Watanabe, Hazuki; Yokoi, Daichi; Watanabe, Hirohisa; Katsuno, Masahisa; Izumi, Yuishin; Taniguchi, Akira; Kanai, Kazuaki; Morita, Mitsuya; Kano, Osamu; Kuwabara, Satoshi; Oda, Masaya; Abe, Koji; Aoki, Masashi; Aiba, Ikuko; Okamoto, Koichi; Mizoguchi, Kouichi; Hattori, Nobutaka; Nakashima, Kenji; Kaji, Ryuji; Sobue, Gen.
Afiliação
  • Nakamura R; Department of Neurology, Nagoya University Graduate School of Medicine, Nagoya, Japan.
  • Tohnai G; Department of Neurology, Nagoya University Graduate School of Medicine, Nagoya, Japan.
  • Atsuta N; Department of Neurology, Nagoya University Graduate School of Medicine, Nagoya, Japan.
  • Nakatochi M; Division of Data Science, Department of Nursing, Nagoya University Graduate School of Medicine, Nagoya, Japan.
  • Hayashi N; Department of Neurology, Nagoya University Graduate School of Medicine, Nagoya, Japan.
  • Watanabe H; Department of Neurology, Nagoya University Graduate School of Medicine, Nagoya, Japan; Department of Neurology, Japanese Red Cross Nagoya Daiichi Hospital, Nagoya, Japan.
  • Yokoi D; Department of Neurology, Nagoya University Graduate School of Medicine, Nagoya, Japan; Department of Neurology, Kakeyu-Misayama Rehabilitation Center Kakeyu Hospital, Ueda, Japan.
  • Watanabe H; Brain and Mind Research Center, Nagoya University, Nagoya, Japan; Department of Neurology, Fujita Health University, Toyoake, Japan.
  • Katsuno M; Department of Neurology, Nagoya University Graduate School of Medicine, Nagoya, Japan.
  • Izumi Y; Department of Neurology, Institute of Biomedical Sciences, Tokushima University Graduate School, Tokushima, Japan.
  • Taniguchi A; Department of Neurology, Mie University Graduate School of Medicine, Tsu, Japan.
  • Kanai K; Department of Neurology, Juntendo University Graduate School of Medicine, Tokyo, Japan; Department of Neurology, Fukushima Medical University School of Medicine, Fukushima, Japan.
  • Morita M; Division of Neurology, Department of Internal Medicine, Jichi Medical University, Shimotsuke, Japan.
  • Kano O; Division of Neurology, Department of Internal Medicine, Toho University Faculty of Medicine, Tokyo, Japan.
  • Kuwabara S; Department of Neurology, Graduate School of Medicine, Chiba University, Chiba, Japan.
  • Oda M; Department of Neurology, Vihara Hananosato Hospital, Miyoshi, Japan.
  • Abe K; Department of Neurology, Okayama University Graduate School of Medicine, Okayama, Japan.
  • Aoki M; Department of Neurology, Tohoku University School of Medicine, Sendai, Japan.
  • Aiba I; Department of Neurology, National Hospital Organization Higashinagoya National Hospital, Nagoya, Japan.
  • Okamoto K; Department of Neurology, Geriatrics Research Institute and Hospital, Maebashi, Japan.
  • Mizoguchi K; Department of Neurology, National Hospital Organization Shizuoka Medical Center, Shizuoka, Japan.
  • Hattori N; Department of Neurology, Juntendo University Graduate School of Medicine, Tokyo, Japan.
  • Nakashima K; Department of Neurology, National Hospital Organization Matsue Medical Center, Matsue, Japan.
  • Kaji R; Department of Neurology, Institute of Biomedical Sciences, Tokushima University Graduate School, Tokushima, Japan.
  • Sobue G; Department of Neurology, Nagoya University Graduate School of Medicine, Nagoya, Japan; Brain and Mind Research Center, Nagoya University, Nagoya, Japan; Aichi Medical University, Nagakute, Japan. Electronic address: sobueg@med.nagoya-u.ac.jp.
Neurobiol Aging ; 97: 147.e11-147.e17, 2021 01.
Article em En | MEDLINE | ID: mdl-32888732
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Cinesinas / Predisposição Genética para Doença / Estudos de Associação Genética / Mutação com Perda de Função / Esclerose Lateral Amiotrófica Tipo de estudo: Clinical_trials Limite: Humans País/Região como assunto: Asia Idioma: En Revista: Neurobiol Aging Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Japão
Texto completo
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XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Cinesinas / Predisposição Genética para Doença / Estudos de Associação Genética / Mutação com Perda de Função / Esclerose Lateral Amiotrófica Tipo de estudo: Clinical_trials Limite: Humans País/Região como assunto: Asia Idioma: En Revista: Neurobiol Aging Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Japão