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. This work was supported in part through the Research Committee of the University of Thessaly (Code: 2845), Institute of Biomedical Research & Technology, CERETETH (Code: 01-04-207), and PENED 03 grant 650, “Genetic Variations of PD Associated Genes in the Greek Population and their Functional Analysis,” from the Hellenic Secretariat of Research and Technology (to D.V. and L.S.). Novartis Hellas was a cosponsor of this grant.
Letters: New Observation
Lack of association of the UCHL-1 gene with Parkinson's disease in a greek cohort: A haplotype-tagging approach†
Article first published online: 28 MAY 2011
DOI: 10.1002/mds.23694
Copyright © 2011 Movement Disorder Society
Additional Information
How to Cite
Xiromerisiou, G., Kyratzi, E., Dardiotis, E., Bozi, M., Tsimourtou, V., Stamboulis, E., Ralli, S., Vassilatis, D., Gourbali, V., Kountra, P.-M., Fountas, K., Papadimitriou, A., Stefanis, L. and Hadjigeorgiou, G. M. (2011), Lack of association of the UCHL-1 gene with Parkinson's disease in a greek cohort: A haplotype-tagging approach. Mov. Disord., 26: 1955–1957. doi: 10.1002/mds.23694
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Publication History
- Issue published online: 26 AUG 2011
- Article first published online: 28 MAY 2011
- Manuscript Accepted: 24 JAN 2011
- Manuscript Revised: 11 JAN 2011
- Manuscript Received: 17 SEP 2010
No abstract is available for this article.

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