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Rare genetic variation in mitochondrial pathways influences the risk for Parkinson's disease.
Gaare, Johannes J; Nido, Gonzalo S; Sztromwasser, Pawel; Knappskog, Per M; Dahl, Olav; Lund-Johansen, Morten; Maple-Grødem, Jodi; Alves, Guido; Tysnes, Ole-Bjørn; Johansson, Stefan; Haugarvoll, Kristoffer; Tzoulis, Charalampos.
Affiliation
  • Gaare JJ; Department of Neurology, Haukeland University Hospital, Bergen, Norway.
  • Nido GS; Department of Clinical Medicine, University of Bergen, Bergen, Norway.
  • Sztromwasser P; Department of Neurology, Haukeland University Hospital, Bergen, Norway.
  • Knappskog PM; Department of Clinical Medicine, University of Bergen, Bergen, Norway.
  • Dahl O; Center for Medical Genetics and Molecular Medicine, Haukeland University Hospital, Bergen, Norway.
  • Lund-Johansen M; Department of Clinical Science, University of Bergen, Bergen, Norway.
  • Maple-Grødem J; Computational Biology Unit, Department of Informatics, University of Bergen, Bergen, Norway.
  • Alves G; Center for Medical Genetics and Molecular Medicine, Haukeland University Hospital, Bergen, Norway.
  • Tysnes OB; K.G. Jebsen Centre for Neuropsychiatric Disorders, Department of Clinical Science, University of Bergen, Bergen, Norway.
  • Johansson S; Department of Clinical Medicine, University of Bergen, Bergen, Norway.
  • Haugarvoll K; Department of Oncology, Haukeland University Hospital, Bergen, Bergen, Norway.
  • Tzoulis C; Department of Clinical Medicine, University of Bergen, Bergen, Norway.
Mov Disord ; 33(10): 1591-1600, 2018 10.
Article in En | MEDLINE | ID: mdl-30256453
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Parkinson Disease / Genetic Variation / DNA, Mitochondrial / Signal Transduction / Genetic Predisposition to Disease / Mitochondria Type of study: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies / Systematic_reviews Limits: Female / Humans / Male Country/Region as subject: America do norte / Europa Language: En Journal: Mov Disord Journal subject: NEUROLOGIA Year: 2018 Document type: Article Affiliation country: Country of publication:
Fulltext
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Parkinson Disease / Genetic Variation / DNA, Mitochondrial / Signal Transduction / Genetic Predisposition to Disease / Mitochondria Type of study: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies / Systematic_reviews Limits: Female / Humans / Male Country/Region as subject: America do norte / Europa Language: En Journal: Mov Disord Journal subject: NEUROLOGIA Year: 2018 Document type: Article Affiliation country: Country of publication: