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Is the MC1R variant p.R160W associated with Parkinson's?
Lubbe, Steven J; Escott-Price, Valentina; Brice, Alexis; Gasser, Thomas; Hardy, John; Heutink, Peter; Sharma, Manu; Wood, Nicholas W; Nalls, Mike; Singleton, Andrew B; Williams, Nigel M; Morris, Huw R.
Afiliação
  • Lubbe SJ; Department of Clinical Neuroscience, Institute of Neurology, University College London, London, United Kingdom.
  • Escott-Price V; Institute of Psychological Medicine and Clinical Neurosciences, Medical Research Council Center for Neuropsychiatric Genetics and Genomics, Department of Psychological Medicine and Neurology, Cardiff University School of Medicine, Cardiff, United Kingdom.
  • Brice A; Inserm U 1127, CNRS UMR 7225, Sorbonne Universités, UPMC Université Paris 06 UMR S 1127, Institut du Cerveau et de la Moelle épinière, ICM, F-75013, Paris, France.
  • Gasser T; Department for Neurodegenerative Diseases, Hertie Institute for Clinical Brain Research, University of Tübingen, Tübingen, Germany and Genome Biology for Neurodegenerative Diseases, German Center for Neurodegenerative Diseases (DZNE), Tübingen, Germany.
  • Hardy J; Department of Molecular Neuroscience, Institute of Neurology, University College London, London, United Kingdom.
  • Heutink P; Reta Lila Weston Institute, University College London Institute of Neurology, London, United Kingdom.
  • Sharma M; Genome Biology for Neurodegenerative Diseases, German Center for Neurodegenerative Diseases (DZNE), Tübingen, Germany.
  • Wood NW; Department of Molecular Neuroscience, Institute of Neurology, University College London, London, United Kingdom.
  • Nalls M; Inserm U 1127, CNRS UMR 7225, Sorbonne Universités, UPMC Université Paris 06 UMR S 1127, Institut du Cerveau et de la Moelle épinière, ICM, F-75013, Paris, France.
  • Singleton AB; UCL Genetics Institute, University College London, London, United Kingdom.
  • Williams NM; Laboratory of Neurogenetics, National Institute on Aging, Bethesda, MD.
  • Morris HR; Laboratory of Neurogenetics, National Institute on Aging, Bethesda, MD.
Ann Neurol ; 79(1): 159-61, 2016 Jan.
Article em En | MEDLINE | ID: mdl-26389967
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Doença de Parkinson / Variação Genética / Predisposição Genética para Doença / Receptor Tipo 1 de Melanocortina / Melanoma Tipo de estudo: Risk_factors_studies Limite: Female / Humans / Male Idioma: En Ano de publicação: 2016 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Doença de Parkinson / Variação Genética / Predisposição Genética para Doença / Receptor Tipo 1 de Melanocortina / Melanoma Tipo de estudo: Risk_factors_studies Limite: Female / Humans / Male Idioma: En Ano de publicação: 2016 Tipo de documento: Article