Spencer, CCA; Plagnol, V; Strange, A; Gardner, M; Paisan-Ruiz, C; Band, G; Barker, RA; Bellenguez, C; Bhatia, K; Blackburn, H; +39 more... Blackwell, JM; Bramon, E; 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; (2011) Dissection of the genetics of Parkinson's disease identifies an additional association 5 ' of SNCA and multiple associated haplotypes at 17q21. Human molecular genetics, 20 (2). pp. 345-353. ISSN 0964-6906 DOI: https://doi.org/10.1093/hmg/ddq469