Your browser doesn't support javascript.
loading
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.
Affiliation
  • 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 in En | MEDLINE | ID: mdl-31148195

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Parkinson Disease Type of study: Prognostic_studies Limits: Humans Language: En Journal: Ann Neurol Year: 2019 Document type: Article Affiliation country: Luxembourg

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Parkinson Disease Type of study: Prognostic_studies Limits: Humans Language: En Journal: Ann Neurol Year: 2019 Document type: Article Affiliation country: Luxembourg