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

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

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

Author:

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

Tübinger Autor(en):

Simón-Sánchez, Javier
Heutink, Peter
Brockmann, Kathrin
Schulte, Claudia
Gasser, Thomas

Published in:

Lancet Neurology (2016), Bd. 15, H. 6, S. 585-596

Verlagsangabe:

Elsevier Science Inc

Language:

English

Full text:

http://dx.doi.org/10.1016/S1474-4422(16)00071-5

ISSN:

1474-4465