Abstract
We report haplotype analysis of the α-synuclein gene in Parkinson's disease (PD), extending earlier reports of an association with a polymorphism within the gene promoter. This analysis showed significant differences in haplotypes between PD cases and controls. Our analyses demonstrate that genetic variability in the α-synuclein gene is a risk factor for the development of PD. These genetic findings are analogous to the tau haplotype over-represented in progressive supranuclear palsy and further extend the similarity in the etiologies and pathogeneses of the synucleinopathies and tauopathies.
Original language | English (US) |
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Pages (from-to) | 1847-1851 |
Number of pages | 5 |
Journal | Human molecular genetics |
Volume | 10 |
Issue number | 17 |
State | Published - Aug 15 2001 |
ASJC Scopus subject areas
- Molecular Biology
- Genetics
- Genetics(clinical)