Publication:

Dissection of the genetics of Parkinson's disease identifies an additional association 5 ' of SNCA and multiple associated haplotypes at 17q21 (2011)

Author(s): Spencer CCA, Plagnol V, Strange A, Gardner M, Paisan-Ruiz C, Band G, Barker RA, Bellenguez C, Bhatia K, Blackburn H, Blackwell JM, Bramon E, Brown MA, Brown MA, Burn D, Casas JP, Chinnery PF, Clarke CE, Corvin A, Craddock N, Deloukas P, Edkins S, Evans J, Freeman C, Gray E, Hardy J, Hudson G, Hunt S, Jankowski J, Langford C, Lees AJ, Markus HS, Mathew CG, McCarthy MI, Morrison KE, Palmer CNA, Pearson JP, Peltonen L, Pirinen M, Plomin R, Potter S, Rautanen A, Sawcer SJ, Su Z, Trembath RC, Viswanathan AC, Williams NW, Morris HR, Donnelly P, Wood NW, UK Parkinson's Dis Consortium, Wellcome Trust Case Control Consor

      • Date: 02-11-2010
      • Journal: Human Molecular Genetics
      • Volume: 20
      • Issue: 2
      • Pages: 345-353
      • Publisher: Oxford University Press
      • Publication type: Article
      • Bibliographic status: Published

      Keywords: GENOME-WIDE ASSOCIATION PROGRESSIVE SUPRANUCLEAR PALSY RISK-FACTORS TAU REGION INVERSION

      Staff

      Professor Patrick Chinnery
      Institute Director

      Dr Gavin Hudson
      Research Fellow