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Publication Detail
GP2: The Global Parkinson's Genetics Program
  • Publication Type:
    Journal article
  • Publication Sub Type:
    Article
  • Authors:
    Tan AH, Noyce A, Carrasco AM, Brice A, Reimer A, Illarionova A, Singleton A, Schumacher-Schuh A, Stecher B, Siddiqi B, Casey B, Fiske B, Pantazis C, Klein C, Bale C, Wegel C, Blauwendraat C, Vitale D, Hernandez D, Riley E, Fisher E, Valente EM, Vollstedt EJ, Faghri F, Leonard H, Iwaki H, Morris H, Sarmiento IJK, Mata I, Kim J, Hardy J, Murphy K, Lohmann K, Marek K, Mok K, Kumar K, Lange L, Kuhl M, Sharma M, Tan M, Makarious M, Durborow M, Avenali M, Rizig M, Nalls M, Mencacci N, Wood N, Williams N, Okubadejo N, Okunoye O, Lewis P, Heutink P, Prashanth LK, Kruger R, Rajan R, Murtadha R, Adams S, Bandres-Ciga S, Fox S, Lim S-Y, Stott S, Bardien S, Foroud T, Gasser T, Sherer T, Song Y, Fang Z-H
  • Publisher:
    WILEY
  • Publication date:
    29/01/2021
  • Journal:
    MOVEMENT DISORDERS
  • Status:
    Published
  • Print ISSN:
    0885-3185
  • Language:
    English
  • Keywords:
    Science & Technology, Life Sciences & Biomedicine, Clinical Neurology, Neurosciences & Neurology, Parkinson's disease, genetics, genome-wide association, mutation, LINKED DYSTONIA-PARKINSONISM, DISEASE, GENOME, RISK, LOCI
Abstract
No abstract found
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Clinical and Movement Neurosciences
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Department of Neuromuscular Diseases
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