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A comprehensive analysis of SNCA-related genetic risk in sporadic parkinson disease.
Pihlstrøm, Lasse; Blauwendraat, Cornelis; Cappelletti, Chiara; Berge-Seidl, Victoria; Langmyhr, Margrete; Henriksen, Sandra Pilar; van de Berg, Wilma D J; Gibbs, J Raphael; Cookson, Mark R; Singleton, Andrew B; Nalls, Mike A; Toft, Mathias.
Afiliação
  • Pihlstrøm L; Department of Neurology, Oslo University Hospital, Oslo, Norway.
  • Blauwendraat C; Neurodegenerative Diseases Research Unit, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD.
  • Cappelletti C; Laboratory of Neurogenetics, National Institute on Aging, National Institutes of Health, Bethesda, MD.
  • Berge-Seidl V; Department of Neurology, Oslo University Hospital, Oslo, Norway.
  • Langmyhr M; Department of Neurology, Oslo University Hospital, Oslo, Norway.
  • Henriksen SP; Department of Neurology, Oslo University Hospital, Oslo, Norway.
  • van de Berg WDJ; Department of Neurology, Oslo University Hospital, Oslo, Norway.
  • Gibbs JR; Department of Anatomy and Neurosciences, Clinical Neuroanatomy Section, Amsterdam Neuroscience, VU Medical Center, Amsterdam, the Netherlands.
  • Cookson MR; Laboratory of Neurogenetics, National Institute on Aging, National Institutes of Health, Bethesda, MD.
  • Nalls MA; Laboratory of Neurogenetics, National Institute on Aging, National Institutes of Health, Bethesda, MD.
  • Toft M; Laboratory of Neurogenetics, National Institute on Aging, National Institutes of Health, Bethesda, MD.
Ann Neurol ; 84(1): 117-129, 2018 07.
Article em En | MEDLINE | ID: mdl-30146727
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doença de Parkinson / Predisposição Genética para Doença / Polimorfismo de Nucleotídeo Único / Alfa-Sinucleína Tipo de estudo: Diagnostic_studies / Etiology_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2018 Tipo de documento: Article
Texto completo
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doença de Parkinson / Predisposição Genética para Doença / Polimorfismo de Nucleotídeo Único / Alfa-Sinucleína Tipo de estudo: Diagnostic_studies / Etiology_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2018 Tipo de documento: Article