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Mitochondrial DNA Deletions Discriminate Affected from Unaffected LRRK2 Mutation Carriers.
Ouzren, Nassima; Delcambre, Sylvie; Ghelfi, Jenny; Seibler, Philip; Farrer, Matthew J; König, Inke R; Aasly, Jan O; Trinh, Joanne; Klein, Christine; Grünewald, Anne.
Afiliação
  • Ouzren N; Luxembourg Centre for Systems Biomedicine, University of Luxembourg, Esch-sur-Alzette, Luxembourg.
  • Delcambre S; Luxembourg Centre for Systems Biomedicine, University of Luxembourg, Esch-sur-Alzette, Luxembourg.
  • Ghelfi J; Luxembourg Centre for Systems Biomedicine, University of Luxembourg, Esch-sur-Alzette, Luxembourg.
  • Seibler P; Institute of Neurogenetics, University of Lübeck, Lübeck, Germany.
  • Farrer MJ; Department of Medical Genetics, University of British Columbia, Vancouver, British Columbia, Canada.
  • König IR; Institute of Medical Biometry and Statistics, University of Lübeck, Lübeck, Germany.
  • Aasly JO; Department of Neuromedicine and Movement Science and Department of Neurology, St Olav's Hospital, Norwegian University of Science and Technology, Trondheim, Norway.
  • Trinh J; Institute of Neurogenetics, University of Lübeck, Lübeck, Germany.
  • Klein C; Institute of Neurogenetics, University of Lübeck, Lübeck, Germany.
  • Grünewald A; Luxembourg Centre for Systems Biomedicine, University of Luxembourg, Esch-sur-Alzette, Luxembourg.
Ann Neurol ; 86(2): 324-326, 2019 08.
Article em En | MEDLINE | ID: mdl-31148195
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doença de Parkinson Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2019 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 Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2019 Tipo de documento: Article