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Letter
A clinical and family history study of Parkinson's disease in heterozygous glucocerebrosidase mutation carriers
- Correspondence to Professor Anthony H V Schapira, Department of Clinical Neurosciences, Rowland Hill St., London NW3 2PF, UK; a.schapira{at}ucl.ac.uk
Citation
A clinical and family history study of Parkinson's disease in heterozygous glucocerebrosidase mutation carriers
Publication history
- Received January 30, 2012
- Revised March 12, 2012
- Accepted March 29, 2012
- First published May 10, 2012.
Online issue publication
July 30, 2016
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© 2012, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions. This is an open-access article distributed under the terms of the Creative Commons Attribution Non-commercial License, which permits use, distribution, and reproduction in any medium, provided the original work is properly cited, the use is non commercial and is otherwise in compliance with the license. See: http://creativecommons.org/licenses/by-nc/3.0/ and http://creativecommons.org/licenses/by-nc/3.0/legalcode