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Fine mapping and resequencing of the PARK16 locus in Parkinson's disease.
Pihlstrøm, Lasse; Rengmark, Aina; Bjørnarå, Kari Anne; Dizdar, Nil; Fardell, Camilla; Forsgren, Lars; Holmberg, Björn; Larsen, Jan Petter; Linder, Jan; Nissbrandt, Hans; Tysnes, Ole-Bjørn; Dietrichs, Espen; Toft, Mathias.
Afiliación
  • Pihlstrøm L; 1] Department of Neurology, Oslo University Hospital, Oslo, Norway [2] University of Oslo, Institute of Clinical Medicine, Oslo, Norway.
  • Rengmark A; Department of Neurology, Oslo University Hospital, Oslo, Norway.
  • Bjørnarå KA; Department of Neurology, Drammen Hospital, Drammen, Norway.
  • Dizdar N; Department of Clinical and Experimental Medicine, Linköping University, Linköping, Sweden.
  • Fardell C; Department of Pharmacology, The Sahlgrenska Academy at University of Gothenburg, Gothenburg, Sweden.
  • Forsgren L; Department of Pharmacology and Clinical Neuroscience, Umeå University, Umeå, Sweden.
  • Holmberg B; Department of Clinical Neuroscience and Rehabilitation, The Sahlgrenska Academy at University of Gothenburg, Gothenburg, Sweden.
  • Larsen JP; The Norwegian Centre for Movement Disorders, Stavanger University Hospital, Stavanger, Norway.
  • Linder J; Department of Pharmacology and Clinical Neuroscience, Umeå University, Umeå, Sweden.
  • Nissbrandt H; Department of Pharmacology, The Sahlgrenska Academy at University of Gothenburg, Gothenburg, Sweden.
  • Tysnes OB; Department of Neurology, Haukeland University Hospital, Bergen, Norway.
  • Dietrichs E; 1] Department of Neurology, Oslo University Hospital, Oslo, Norway [2] University of Oslo, Institute of Clinical Medicine, Oslo, Norway.
  • Toft M; Department of Neurology, Oslo University Hospital, Oslo, Norway.
J Hum Genet ; 60(7): 357-62, 2015 Jul.
Article en En | MEDLINE | ID: mdl-25855069

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Enfermedad de Parkinson Tipo de estudio: Observational_studies / Risk_factors_studies / Systematic_reviews Límite: Humans Idioma: En Revista: J Hum Genet Asunto de la revista: GENETICA MEDICA Año: 2015 Tipo del documento: Article País de afiliación: Noruega

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Enfermedad de Parkinson Tipo de estudio: Observational_studies / Risk_factors_studies / Systematic_reviews Límite: Humans Idioma: En Revista: J Hum Genet Asunto de la revista: GENETICA MEDICA Año: 2015 Tipo del documento: Article País de afiliación: Noruega