Members of the French Parkinson Disease Genetic Group are listed in the Appendix on page 471.
G51D α-synuclein mutation causes a novel Parkinsonian–pyramidal syndrome
Version of Record online: 21 MAY 2013
Copyright © 2013 American Neurological Association
Annals of Neurology
Volume 73, Issue 4, pages 459–471, April 2013
How to Cite
Lesage, S., Anheim, M., Letournel, F., Bousset, L., Honoré, A., Rozas, N., Pieri, L., Madiona, K., Dürr, A., Melki, R., Verny, C., Brice, A. and for the French Parkinson's Disease Genetics Study Group (2013), G51D α-synuclein mutation causes a novel Parkinsonian–pyramidal syndrome. Ann Neurol., 73: 459–471. doi: 10.1002/ana.23894
- Issue online: 21 MAY 2013
- Version of Record online: 21 MAY 2013
- Accepted manuscript online: 22 MAR 2013 08:39PM EST
- Manuscript Accepted: 5 MAR 2013
- Manuscript Revised: 18 FEB 2013
- Manuscript Received: 18 OCT 2012
Additional Supporting Information may be found in the online version of this article.
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