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Mutations in bassoon in individuals with familial and sporadic progressive supranuclear palsy-like syndrome.
Yabe, Ichiro; Yaguchi, Hiroaki; Kato, Yasutaka; Miki, Yasuo; Takahashi, Hidehisa; Tanikawa, Satoshi; Shirai, Shinichi; Takahashi, Ikuko; Kimura, Mari; Hama, Yuka; Matsushima, Masaaki; Fujioka, Shinsuke; Kano, Takahiro; Watanabe, Masashi; Nakagawa, Shin; Kunieda, Yasuyuki; Ikeda, Yoshio; Hasegawa, Masato; Nishihara, Hiroshi; Ohtsuka, Toshihisa; Tanaka, Shinya; Tsuboi, Yoshio; Hatakeyama, Shigetsugu; Wakabayashi, Koichi; Sasaki, Hidenao.
Afiliación
  • Yabe I; Department of Neurology, Faculty of Medicine and Graduate School of Medicine, Hokkaido University, Sapporo, Japan. yabe@med.hokudai.ac.jp.
  • Yaguchi H; Department of Neurology, Faculty of Medicine and Graduate School of Medicine, Hokkaido University, Sapporo, Japan.
  • Kato Y; Department of Biochemistry, Faculty of Medicine and Graduate School of Medicine, Hokkaido University, Sapporo, Japan.
  • Miki Y; Department of Cancer Pathology, Faculty of Medicine and Graduate School of Medicine, Hokkaido University, Sapporo, Japan.
  • Takahashi H; Laboratory of Oncology, Hokuto Hospital, Obihiro, Japan.
  • Tanikawa S; Department of Neuropathology, Hirosaki University Graduate School of Medicine, Hirosaki, Japan.
  • Shirai S; Department of Biochemistry, Faculty of Medicine and Graduate School of Medicine, Hokkaido University, Sapporo, Japan.
  • Takahashi I; Department of Cancer Pathology, Faculty of Medicine and Graduate School of Medicine, Hokkaido University, Sapporo, Japan.
  • Kimura M; Department of Neurology, Faculty of Medicine and Graduate School of Medicine, Hokkaido University, Sapporo, Japan.
  • Hama Y; Department of Neurology, Faculty of Medicine and Graduate School of Medicine, Hokkaido University, Sapporo, Japan.
  • Matsushima M; Department of Neurology, Faculty of Medicine and Graduate School of Medicine, Hokkaido University, Sapporo, Japan.
  • Fujioka S; Department of Neurology, Faculty of Medicine and Graduate School of Medicine, Hokkaido University, Sapporo, Japan.
  • Kano T; Department of Neurology, Faculty of Medicine and Graduate School of Medicine, Hokkaido University, Sapporo, Japan.
  • Watanabe M; Department of Neurology, Fukuoka University School of Medicine, Fukuoka, Japan.
  • Nakagawa S; Department of Neurology, Faculty of Medicine and Graduate School of Medicine, Hokkaido University, Sapporo, Japan.
  • Kunieda Y; Department of Biochemistry, Faculty of Medicine and Graduate School of Medicine, Hokkaido University, Sapporo, Japan.
  • Ikeda Y; Department of Psychiatry, Faculty of Medicine and Graduate School of Medicine, Hokkaido University, Sapporo, Japan.
  • Hasegawa M; Wakkanai City Hospital, Wakkanai, Japan.
  • Nishihara H; Department of Neurology, Gunma University Graduate School of Medicine, Maebashi, Japan.
  • Ohtsuka T; Department of Dementia and Higher Brain Function, Tokyo Metropolitan Institute of Medical Science, Tokyo, Japan.
  • Tanaka S; Department of Cancer Pathology, Faculty of Medicine and Graduate School of Medicine, Hokkaido University, Sapporo, Japan.
  • Tsuboi Y; Division of Clinical Cancer Genomics, Cancer Center, Keio University School of Medicine, Tokyo, Japan.
  • Hatakeyama S; Department of Biochemistry, Faculty of Medicine/Graduate School of Medicine, University of Yamanashi, Chuo, Japan.
  • Wakabayashi K; Department of Cancer Pathology, Faculty of Medicine and Graduate School of Medicine, Hokkaido University, Sapporo, Japan.
  • Sasaki H; Global Station for Soft Matter, Global Institution for Collaborative Research and Education, Hokkaido University, Sapporo, Japan.
Sci Rep ; 8(1): 819, 2018 01 16.
Article en En | MEDLINE | ID: mdl-29339765
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Parálisis Supranuclear Progresiva / Salud de la Familia / Mutación Missense / Proteínas del Tejido Nervioso Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Revista: Sci Rep Año: 2018 Tipo del documento: Article País de afiliación: Japón Pais de publicación: Reino Unido
Texto completo
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XML
PubMed Links
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Parálisis Supranuclear Progresiva / Salud de la Familia / Mutación Missense / Proteínas del Tejido Nervioso Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Revista: Sci Rep Año: 2018 Tipo del documento: Article País de afiliación: Japón Pais de publicación: Reino Unido