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CHCHD2 mutations in autosomal dominant late-onset Parkinson's disease: a genome-wide linkage and sequencing study.
Funayama, Manabu; Ohe, Kenji; Amo, Taku; Furuya, Norihiko; Yamaguchi, Junji; Saiki, Shinji; Li, Yuanzhe; Ogaki, Kotaro; Ando, Maya; Yoshino, Hiroyo; Tomiyama, Hiroyuki; Nishioka, Kenya; Hasegawa, Kazuko; Saiki, Hidemoto; Satake, Wataru; Mogushi, Kaoru; Sasaki, Ryogen; Kokubo, Yasumasa; Kuzuhara, Shigeki; Toda, Tatsushi; Mizuno, Yoshikuni; Uchiyama, Yasuo; Ohno, Kinji; Hattori, Nobutaka.
Afiliación
  • Funayama M; Research Institute for Diseases of Old Age, Graduate School of Medicine, Juntendo University, Tokyo, Japan; Department of Neurology, Juntendo University School of Medicine, Tokyo, Japan.
  • Ohe K; Division of Neurogenetics, Center for Neurological Diseases and Cancer, Nagoya University Graduate School of Medicine, Nagoya, Japan; Training Program of Leaders for Integrated Medical System for Fruitful Healthy-Longevity Society (LIMS), Kyoto University Graduate School of Medicine, Kyoto, Japan.
  • Amo T; Department of Applied Chemistry, National Defense Academy, Yokosuka, Japan.
  • Furuya N; Department of Research and Therapeutics for Movement Disorders, Graduate School of Medicine, Juntendo University, Tokyo, Japan; Department of Neurology, Juntendo University School of Medicine, Tokyo, Japan.
  • Yamaguchi J; Department of Cellular and Molecular Neuropathology, Juntendo University School of Medicine, Tokyo, Japan.
  • Saiki S; Department of Neurology, Juntendo University School of Medicine, Tokyo, Japan.
  • Li Y; Department of Neurology, Juntendo University School of Medicine, Tokyo, Japan.
  • Ogaki K; Department of Neurology, Juntendo University School of Medicine, Tokyo, Japan.
  • Ando M; Department of Neurology, Juntendo University School of Medicine, Tokyo, Japan.
  • Yoshino H; Research Institute for Diseases of Old Age, Graduate School of Medicine, Juntendo University, Tokyo, Japan.
  • Tomiyama H; Department of Neurology, Juntendo University School of Medicine, Tokyo, Japan.
  • Nishioka K; Department of Neurology, Juntendo University School of Medicine, Tokyo, Japan.
  • Hasegawa K; Department of Neurology, National Hospital Organization, Sagamihara National Hospital, Sagamihara, Japan.
  • Saiki H; Department of Neurology, Tazuke Kofukai Medical Research Institute and Kitano Hospital, Osaka, Japan.
  • Satake W; Division of Neurology and Molecular Brain Science, Kobe University Graduate School of Medicine, Kobe, Japan.
  • Mogushi K; Center for Genomic and Regenerative Medicine, Juntendo University School of Medicine, Tokyo, Japan.
  • Sasaki R; Department of Neurology, Mie University Graduate School of Medicine, Tsu, Japan.
  • Kokubo Y; Kii ALS/PDC Research Center, Mie University Graduate School of Regional Innovation Studies, Tsu, Japan.
  • Kuzuhara S; Department of Neurology and Medicine, School of Nursing, Suzuka University of Medical Science, Suzuka, Japan.
  • Toda T; Division of Neurology and Molecular Brain Science, Kobe University Graduate School of Medicine, Kobe, Japan.
  • Mizuno Y; Department of Neurology, Juntendo University School of Medicine, Tokyo, Japan.
  • Uchiyama Y; Research Institute for Diseases of Old Age, Graduate School of Medicine, Juntendo University, Tokyo, Japan; Department of Cellular and Molecular Neuropathology, Juntendo University School of Medicine, Tokyo, Japan.
  • Ohno K; Division of Neurogenetics, Center for Neurological Diseases and Cancer, Nagoya University Graduate School of Medicine, Nagoya, Japan.
  • Hattori N; Research Institute for Diseases of Old Age, Graduate School of Medicine, Juntendo University, Tokyo, Japan; Department of Neurology, Juntendo University School of Medicine, Tokyo, Japan. Electronic address: nhattori@juntendo.ac.jp.
Lancet Neurol ; 14(3): 274-82, 2015 Mar.
Article en En | MEDLINE | ID: mdl-25662902
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Factores de Transcripción / Análisis de Secuencia de ADN / Mutación Missense / Trastornos Parkinsonianos / Proteínas Mitocondriales / Estudio de Asociación del Genoma Completo / Ligamiento Genético Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Lancet Neurol Asunto de la revista: NEUROLOGIA Año: 2015 Tipo del documento: Article País de afiliación: Japón
Texto completo
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XML
PubMed Links
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Factores de Transcripción / Análisis de Secuencia de ADN / Mutación Missense / Trastornos Parkinsonianos / Proteínas Mitocondriales / Estudio de Asociación del Genoma Completo / Ligamiento Genético Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Lancet Neurol Asunto de la revista: NEUROLOGIA Año: 2015 Tipo del documento: Article País de afiliación: Japón