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

C.C.A. Spencer, V. Plagnol, A. Strange, M. Gardner, C. Paisan-Ruiz, G. Band, R.A. Barker, C. Bellenguez, K. Bhatia, H. Blackburn, J.M. Blackwell, E. Bramon, M.A. Brown, D. Burn, J.-P. Casas, P.F. Chinnery, C.E. Clarke, A. Corvin, N. Craddock, P. DeloukasS. Edkins, J. Evans, C. Freeman, E. Gray, J. Hardy, G. Hudson, S. Hunt, J. Jankowski, C. Langford, A.J. Lees, H.S. Markus, C.G. Mathew, M.I. McCarthy, K.E. Morrison, C.N.A. Palmer, J.P. Pearson, L. Peltonen, M. Pirinen, R. Plomin, S. Potter, A. Rautanen, S.J. Sawcer, Z. Su, R.C. Trembath, A.C. Viswanathan, N.W. Williams, H.R. Morris, P. Donnelly, N.W. Wood

Research output: Contribution to journalArticlepeer-review

166 Citations (Scopus)
Original languageEnglish
Pages (from-to)345-353
Number of pages9
JournalHuman Molecular Genetics
Issue number2
Publication statusPublished - 15 Jan 2011

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