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Association of ATXN2 intermediate-length CAG repeats with amyotrophic lateral sclerosis correlates with the distributions of normal CAG repeat alleles among individual ethnic populations.
Naruse, Hiroya; Matsukawa, Takashi; Ishiura, Hiroyuki; Mitsui, Jun; Takahashi, Yuji; Takano, Hiroki; Goto, Jun; Toda, Tatsushi; Tsuji, Shoji.
Afiliación
  • Naruse H; Department of Neurology, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
  • Matsukawa T; Department of Neurology, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
  • Ishiura H; Department of Molecular Neurology, Graduate School of Medicine, The University of Tokyo, 7-3-1 Hongo, Bunkyo, Tokyo, 113-8655, Japan.
  • Mitsui J; Department of Neurology, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
  • Takahashi Y; Department of Neurology, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
  • Takano H; Department of Molecular Neurology, Graduate School of Medicine, The University of Tokyo, 7-3-1 Hongo, Bunkyo, Tokyo, 113-8655, Japan.
  • Goto J; Department of Neurology, National Center Hospital, National Center of Neurology and Psychiatry, Tokyo, Japan.
  • Toda T; Department of Neurology, Tachikawa General Hospital, Niigata, Japan.
  • Tsuji S; Department of Neurology, International University of Health and Welfare Mita Hospital, Tokyo, Japan.
Neurogenetics ; 20(2): 65-71, 2019 05.
Article en En | MEDLINE | ID: mdl-30847648
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Alelos / Ataxina-2 / Esclerosis Amiotrófica Lateral Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies País/Región como asunto: Asia Idioma: En Revista: Neurogenetics Asunto de la revista: GENETICA / NEUROLOGIA Año: 2019 Tipo del documento: Article
Texto completo
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Alelos / Ataxina-2 / Esclerosis Amiotrófica Lateral Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies País/Región como asunto: Asia Idioma: En Revista: Neurogenetics Asunto de la revista: GENETICA / NEUROLOGIA Año: 2019 Tipo del documento: Article