Deletions at 22q11.2 in idiopathic Parkinson's disease: a combined analysis of genome-wide association data

Kin Y. Mok, Una Sheerin, Javier Simon-Sanchez, Afnan Salaka, Lucy Chester, Valentina Escott-Price, Kiran Mantripragada, Karen M. Doherty, Alastair J. Noyce, Niccolo E. Mencacci, Steven J. Lubbe, Caroline H. Williams-Gray, Roger A. Barker, Karin van Dijk, Henk W. Berendse, Peter Heutink, Jean-Christophe Corvol, Florence Cormier, Suzanne Lesage, Alexis BriceKathrin Brockmann, Claudia Schulte, Thomas Gasser, Thomas Foltynie, Patricia Limousin, Karen E. Morrison, Carl E. Clarke, Stephen Sawcer, Tom T. Warner, Andrew J. Lees, Huw R. Morris, Mike A. Nalls, Andrew B. Singleton, John Hardy, Andrey Y. Abramov, Vincent Plagnol, Nigel M. Williams, Nicholas W. Wood

Research output: Contribution to journalArticleAcademicpeer-review

Original languageEnglish
Pages (from-to)585-596
JournalLancet Neurology
Volume15
Issue number6
DOIs
Publication statusPublished - May 2016

Cite this

Mok, K. Y., Sheerin, U., Simon-Sanchez, J., Salaka, A., Chester, L., Escott-Price, V., ... Wood, N. W. (2016). Deletions at 22q11.2 in idiopathic Parkinson's disease: a combined analysis of genome-wide association data. Lancet Neurology, 15(6), 585-596. https://doi.org/10.1016/S1474-4422(16)00071-5