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dc.creator | Xiromerisiou, G. | en |
dc.creator | Kyratzi, E. | en |
dc.creator | Dardiotis, E. | en |
dc.creator | Bozi, M. | en |
dc.creator | Tsimourtou, V. | en |
dc.creator | Stamboulis, E. | en |
dc.creator | Ralli, S. | en |
dc.creator | Vassilatis, D. | en |
dc.creator | Gourbali, V. | en |
dc.creator | Kountra, P. M. | en |
dc.creator | Fountas, K. | en |
dc.creator | Papadimitriou, A. | en |
dc.creator | Stefanis, L. | en |
dc.creator | Hadjigeorgiou, G. M. | en |
dc.date.accessioned | 2015-11-23T10:54:20Z | |
dc.date.available | 2015-11-23T10:54:20Z | |
dc.date.issued | 2011 | |
dc.identifier | 10.1002/mds.23694 | |
dc.identifier.issn | 0885-3185 | |
dc.identifier.uri | http://hdl.handle.net/11615/34713 | |
dc.source | Movement Disorders | en |
dc.source.uri | <Go to ISI>://WOS:000295024700033 | |
dc.subject | SUSCEPTIBILITY GENE | en |
dc.subject | S18Y | en |
dc.subject | VARIANT | en |
dc.subject | Clinical Neurology | en |
dc.title | Lack of Association of the UCHL-1 Gene with Parkinson's Disease in a Greek Cohort: A Haplotype-Tagging Approach | en |
dc.type | journalArticle | en |
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