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Mutations in the CHCHD10 gene are a common cause of familial amyotrophic lateral sclerosis.
Johnson, Janel O; Glynn, Shannon M; Gibbs, J Raphael; Nalls, Mike A; Sabatelli, Mario; Restagno, Gabriella; Drory, Vivian E; Chiò, Adriano; Rogaeva, Ekaterina; Traynor, Bryan J.
Afiliação
  • Johnson JO; 1 Neuromuscular Diseases Research Section, Laboratory of Neurogenetics, National Institute on Aging, Bethesda, MD 20892, USA.
  • Glynn SM; 1 Neuromuscular Diseases Research Section, Laboratory of Neurogenetics, National Institute on Aging, Bethesda, MD 20892, USA.
  • Gibbs JR; 2 Computational Biology Core, Laboratory of Neurogenetics, National Institute on Aging, Bethesda, MD 20892, USA.
  • Nalls MA; 3 Molecular Genetics Section, Laboratory of Neurogenetics, National Institute on Aging, Bethesda, MD 20892, USA.
  • Sabatelli M; 4 Neurological Institute, Catholic University and Insieme Contro le Malattie del Motoneurone Association for ALS Research, Largo Agostino Gemelli 8, Rome 00168, Italy.
  • Restagno G; 5 Molecular Genetics Unit, Department of Clinical Pathology, Azienda Sanitaria Ospedaliera Ospedale Infantile Regina Margherita-Santa Anna, Turin 10126, Italy.
  • Drory VE; 6 Department of Neurology, Sourasky Medical Centre, 6 Weizmann Street, Tel Aviv 64239, Israel.
  • Chiò A; 7 'Rita Levi Montalcini' Department of Neuroscience, University of Turin, Turin 10124, Italy.
  • Rogaeva E; 8 Tanz Centre for Research of Neurodegenerative Diseases, Division of Neurology, Department of Medicine, University of Toronto, Toronto, Ontario M5S 3H2, Canada.
  • Traynor BJ; 1 Neuromuscular Diseases Research Section, Laboratory of Neurogenetics, National Institute on Aging, Bethesda, MD 20892, USA traynorb@mail.nih.gov.
Brain ; 137(Pt 12): e311, 2014 Dec.
Article em En | MEDLINE | ID: mdl-25261972
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: DNA Mitocondrial / Doenças Mitocondriais / Proteínas Mitocondriais / Demência Frontotemporal / Esclerose Lateral Amiotrófica / Mitocôndrias Idioma: En Ano de publicação: 2014 Tipo de documento: Article
Texto completo
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XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: DNA Mitocondrial / Doenças Mitocondriais / Proteínas Mitocondriais / Demência Frontotemporal / Esclerose Lateral Amiotrófica / Mitocôndrias Idioma: En Ano de publicação: 2014 Tipo de documento: Article