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Mov Disord. 2009 Dec 15;24(16):2411-4. doi: 10.1002/mds.22795.

Alpha-synuclein polymorphisms are associated with Parkinson's disease in a Saskatchewan population.

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1
Division of Neurology, University of Saskatchewan and Saskatoon Health Region, Saskatoon, Saskatchewan, Canada.

Abstract

Alpha-synuclein gene (SNCA) mutations cause familial Parkinsonism but the role of SNCA variability in idiopathic Parkinson's disease (PD) remains incompletely defined. We report a study of SNCA genetic variation in 452 idiopathic PD cases and 245 controls. SNCA copy number mutations were not associated with early-onset disease in this population. The minor allele "G" at rs356165 was associated with increased odds of PD (P = 0.013) and genetic variation in D4S3481 (Rep1) was associated with age of disease onset (P = 0.007). There was a trend toward association between variation at rs2583988 and rapid PD progression.

PMID:
19890971
DOI:
10.1002/mds.22795
[Indexed for MEDLINE]
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