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

Kin Y. Mok, Una Sheerin, Javier Simón-Sánchez, 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 D. 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*, International Parkinson's Disease Genomics Consortium (IPDGC)

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

75 Scopus citations

Fingerprint

Dive into the research topics of 'Deletions at 22q11.2 in idiopathic Parkinson's disease: A combined analysis of genome-wide association data'. Together they form a unique fingerprint.

Keyphrases

Biochemistry, Genetics and Molecular Biology