Funding agencies: This work was supported by grants from the Parkinson's disease Foundation; Department of Veterans Affairs (1I01BX000531), National Institutes of Health (P50 NS062684, R01 NS065070 and R25 TW009345), Fondo de Investigacion Sanitaria (FIS, PI11/00228, PFIS, FI 11/00259, IFIMAV, and WLA 04/11), Instituto de Salud Carlos III (PI11/00093 and PI08/0915), Spanish Ministry of Economy and Competitiveness, European Social Fund, and the Asociación Parkinson Asturias.
Letters: New Observations
Novel Lrrk2-p.S1761R mutation is not a common cause of Parkinson's disease in Spain
Version of Record online: 6 FEB 2013
Copyright © 2012 Movement Disorder Society
Volume 28, Issue 2, page 248, February 2013
How to Cite
Mata, I. F., Alvarez, V., Ribacoba, R., Infante, J., Sierra, M., Gómez-Garre, P., Mir, P., Waldherr, S., Yearout, D. and Zabetian, C. P. (2013), Novel Lrrk2-p.S1761R mutation is not a common cause of Parkinson's disease in Spain. Mov. Disord., 28: 248. doi: 10.1002/mds.25293
Membership list of the Latin American Research Consortium on the Genetics of Parkinson's Disease is provided in the Supporting Information.
Relevant conflicts of interest/financial disclosures: Nothing to report.
Full financial disclosures and author roles may be found in the online version of this article.
- Issue online: 23 FEB 2013
- Version of Record online: 6 FEB 2013
- Manuscript Accepted: 14 OCT 2012
- Manuscript Revised: 30 SEP 2012
- Manuscript Received: 3 AUG 2012
Additional Supporting Information may be found in the online version of this article.
|mds25293-sup-0001-suppinfo.doc||31K||Suppl. Table 1. Demographic characteristics of the case-control series|
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