Your browser doesn't support javascript.
loading
Defining the causes of sporadic Parkinson's disease in the global Parkinson's genetics program (GP2).
Towns, Clodagh; Richer, Madeleine; Jasaityte, Simona; Stafford, Eleanor J; Joubert, Julie; Antar, Tarek; Martinez-Carrasco, Alejandro; Makarious, Mary B; Casey, Bradford; Vitale, Dan; Levine, Kristin; Leonard, Hampton; Pantazis, Caroline B; Screven, Laurel A; Hernandez, Dena G; Wegel, Claire E; Solle, Justin; Nalls, Mike A; Blauwendraat, Cornelis; Singleton, Andrew B; Tan, Manuela M X; Iwaki, Hirotaka; Morris, Huw R.
Afiliación
  • Towns C; Department of Clinical and Movement Neurosciences, Queen Square Institute of Neurology, University College London, London, UK.
  • Richer M; Department of Clinical and Movement Neurosciences, Queen Square Institute of Neurology, University College London, London, UK.
  • Jasaityte S; Department of Clinical and Movement Neurosciences, Queen Square Institute of Neurology, University College London, London, UK.
  • Stafford EJ; Department of Clinical and Movement Neurosciences, Queen Square Institute of Neurology, University College London, London, UK.
  • Joubert J; University College London, London, UK.
  • Antar T; Department of Clinical and Movement Neurosciences, Queen Square Institute of Neurology, University College London, London, UK.
  • Martinez-Carrasco A; Molecular Genetics Section, Laboratory of Neurogenetics, National Institute on Aging, National Institutes of Health, Bethesda, MD, USA.
  • Makarious MB; Department of Clinical and Movement Neurosciences, Queen Square Institute of Neurology, University College London, London, UK.
  • Casey B; University College London, London, UK.
  • Vitale D; Department of Clinical and Movement Neurosciences, Queen Square Institute of Neurology, University College London, London, UK.
  • Levine K; Molecular Genetics Section, Laboratory of Neurogenetics, National Institute on Aging, National Institutes of Health, Bethesda, MD, USA.
  • Leonard H; National Institutes of Health, Bethesda, MD, USA.
  • Pantazis CB; Department of Clinical Research, Michael J. Fox Foundation for Parkinson's Research, New York City, NY, USA.
  • Screven LA; The Michael J. Fox Foundation for Parkinson's Research, New York, NY, USA.
  • Hernandez DG; National Institutes of Health, Bethesda, MD, USA.
  • Wegel CE; Center for Alzheimer's and Related Dementias (CARD), National Institute on Aging and National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD, USA.
  • Solle J; Data Tecnica International, Washington, DC, USA.
  • Nalls MA; Center for Alzheimer's and Related Dementias (CARD), National Institute on Aging and National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD, USA.
  • Blauwendraat C; Data Tecnica International, Washington, DC, USA.
  • Singleton AB; Molecular Genetics Section, Laboratory of Neurogenetics, National Institute on Aging, National Institutes of Health, Bethesda, MD, USA.
  • Tan MMX; Center for Alzheimer's and Related Dementias (CARD), National Institute on Aging and National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD, USA.
  • Iwaki H; Data Tecnica International, Washington, DC, USA.
  • Morris HR; National Institute on Aging/National Institutes of Health, Bethesda, MD, USA.
NPJ Parkinsons Dis ; 9(1): 131, 2023 Sep 12.
Article en En | MEDLINE | ID: mdl-37699923

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Tipo de estudio: Etiology_studies Idioma: En Revista: NPJ Parkinsons Dis Año: 2023 Tipo del documento: Article País de afiliación: Reino Unido

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Tipo de estudio: Etiology_studies Idioma: En Revista: NPJ Parkinsons Dis Año: 2023 Tipo del documento: Article País de afiliación: Reino Unido