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

UK Parkinson's Disease Consortium; Wellcome Trust Case Control Consortium 2; Spencer, Chris CA; Plagnol, Vincent; Strange, Amy; Gardner, Michelle; Paisan-Ruiz, Coro; Band, Gavin; Barker, Roger A; Bellenguez, Celine; +42 more... Bhatia, Kailash; Blackburn, Hannah; Blackwell, Jennie M; Bramon, Elvira; Brown, Martin A; Brown, Matthew A; Burn, David; Casas, Juan-Pablo; Chinnery, Patrick F; Clarke, Carl E; Corvin, Aiden; Craddock, Nicholas; Deloukas, Panos; Edkins, Sarah; Evans, Jonathan; Freeman, Colin; Gray, Emma; Hardy, John; Hudson, Gavin; Hunt, Sarah; Jankowski, Janusz; Langford, Cordelia; Lees, Andrew J; Markus, Hugh S; Mathew, Christopher G; McCarthy, Mark I; Morrison, Karen E; Palmer, Colin NA; Pearson, Justin P; Peltonen, Leena; Pirinen, Matti; Plomin, Robert; Potter, Simon; Rautanen, Anna; Sawcer, Stephen J; Su, Zhan; Trembath, Richard C; Viswanathan, Ananth C; Williams, Nigel W; Morris, Huw R; Donnelly, Peter; Wood, Nicholas W; (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

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