1. Volume 15, Issue 6, Pages 585-596 (May 2016)
Deletions at 22q11.2 in idiopathic Parkinson's disease: a combined analysis of genome- wide association data 
Kin Y Mok, FRCP, Una Sheerin, MRCP, Javier Simón-Sánchez, PhD, Afnan Salaka, PhD, Lucy Chester, MPharm, Valentina Escott- Price, PhD, Kiran Mantripragada, PhD, Karen M Doherty, MD, Alastair J Noyce, MRCP, Niccolo E Mencacci, MD, Steven J Lubbe, PhD, Caroline H Williams-Gray, PhD, Prof Roger A Barker, PhD, Karin D van Dijk, MD, Prof Henk W Berendse, MD, Prof Peter Heutink, PhD, Prof Jean-Christophe Corvol, MD, Florence Cormier, MD, Suzanne Lesage, PhD, Prof Alexis Brice, MD, Kathrin Brockmann, MD, Claudia Schulte, PhD, Prof Thomas Gasser, MD, Thomas Foltynie, PhD, Prof Patricia Limousin, PhD, Prof Karen E Morrison, DPhil, Prof Carl E Clarke, FRCP, Prof Stephen Sawcer, PhD, Prof Tom T Warner, FRCP, Prof Andrew J Lees, FRCP, Prof Huw R Morris, FRCP, Mike A Nalls, PhD, Andrew B Singleton, PhD, Prof John Hardy, PhD, Prof Andrey Y Abramov, PhD, Vincent Plagnol, PhD, Dr Nigel M Williams, PhD, Prof Nicholas W Wood, FRCP 
The Lancet Neurology 
Volume 15, Issue 6, Pages (May 2016)
DOI: /S (16)
Copyright © 2016 Mok et al. Open Access article distributed under the terms of CC BY Terms and Conditions

2. Figure
Genomic location of the 22q11.2 deletions found in the eight patients with Parkinson's disease and location of the low copy repeat regions
UK3 represented an atypical deletion of uncertain relation to 22q11.2 deletion syndrome and was not considered here. Figure drawn using the UCSC Genome Browser.24
The Lancet Neurology  , DOI: ( /S (16) )
Copyright © 2016 Mok et al. Open Access article distributed under the terms of CC BY Terms and Conditions