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Genetic analysis of ATP10B for Parkinson's disease in Japan.
Ishiguro, Mayu; Yoshino, Hiroyo; Li, Yuanzhe; Ikeda, Aya; Funayama, Manabu; Nishioka, Kenya; Hattori, Nobutaka.
Afiliación
  • Ishiguro M; Department of Neurology, Juntendo University School of Medicine, 2-1-1 Hongo, Bunkyo-ku, Tokyo, 113-8421, Japan. Electronic address: my-sakurai@juntendo.ac.jp.
  • Yoshino H; Research Institute for Diseases of Old Age, Graduate School of Medicine, Juntendo University, 2-1-1 Hongo, Bunkyo-ku, Tokyo, 113-8421, Japan. Electronic address: yhiroyo@juntendo.ac.jp.
  • Li Y; Department of Neurology, Juntendo University School of Medicine, 2-1-1 Hongo, Bunkyo-ku, Tokyo, 113-8421, Japan. Electronic address: yuanzhe@juntendo.ac.jp.
  • Ikeda A; Department of Neurology, Juntendo University School of Medicine, 2-1-1 Hongo, Bunkyo-ku, Tokyo, 113-8421, Japan. Electronic address: amanabe@juntendo.ac.jp.
  • Funayama M; Department of Neurology, Juntendo University School of Medicine, 2-1-1 Hongo, Bunkyo-ku, Tokyo, 113-8421, Japan; Research Institute for Diseases of Old Age, Graduate School of Medicine, Juntendo University, 2-1-1 Hongo, Bunkyo-ku, Tokyo, 113-8421, Japan. Electronic address: funayama@juntendo.ac.jp.
  • Nishioka K; Department of Neurology, Juntendo University School of Medicine, 2-1-1 Hongo, Bunkyo-ku, Tokyo, 113-8421, Japan. Electronic address: nishioka@juntendo.ac.jp.
  • Hattori N; Department of Neurology, Juntendo University School of Medicine, 2-1-1 Hongo, Bunkyo-ku, Tokyo, 113-8421, Japan; Research Institute for Diseases of Old Age, Graduate School of Medicine, Juntendo University, 2-1-1 Hongo, Bunkyo-ku, Tokyo, 113-8421, Japan. Electronic address: nhattori@juntendo.ac.jp.
Parkinsonism Relat Disord ; 88: 10-12, 2021 07.
Article en En | MEDLINE | ID: mdl-34091411
Compound heterozygosity of ATP10B is thought to be a risk factor for young-onset Parkinson's disease (PD). We genetically screened 245 patients with young-onset sporadic PD and 33 patients with autosomal recessive PD for ATP10B. All 13 identified gene variants were heterozygous with little evidence of the pathogenicity.
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Enfermedad de Parkinson / Proteínas de Transporte de Membrana / Adenosina Trifosfatasas Tipo de estudio: Etiology_studies / Prognostic_studies / Risk_factors_studies País/Región como asunto: Asia Idioma: En Revista: Parkinsonism Relat Disord Asunto de la revista: NEUROLOGIA Año: 2021 Tipo del documento: Article
Texto completo
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Enfermedad de Parkinson / Proteínas de Transporte de Membrana / Adenosina Trifosfatasas Tipo de estudio: Etiology_studies / Prognostic_studies / Risk_factors_studies País/Región como asunto: Asia Idioma: En Revista: Parkinsonism Relat Disord Asunto de la revista: NEUROLOGIA Año: 2021 Tipo del documento: Article