Festination Correlates with SNCA Polymorphism in Chinese Patients with Parkinson’s Disease
The genetic basis of festination, a common motor symptom in Parkinson’s disease (PD), remains unclear. Since polymorphism in the alpha-synuclein (SNCA) gene is associated with PD phenotype, we examined whether such polymorphism is also associated with festination. SNCA polymorphisms rs11931074 and r...
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Veröffentlicht in: | Parkinson's disease 2017-01, Vol.2017 (2017), p.1-4 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | The genetic basis of festination, a common motor symptom in Parkinson’s disease (PD), remains unclear. Since polymorphism in the alpha-synuclein (SNCA) gene is associated with PD phenotype, we examined whether such polymorphism is also associated with festination. SNCA polymorphisms rs11931074 and rs894278 were genotyped in a consecutive series of 258 patients with PD, of whom 122 (47.3%) suffered festination. Univariate analysis revealed significant differences in genotype and minor allele frequencies at rs11931074 or rs894278 between patients with festination and those without it (all p |
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ISSN: | 2090-8083 2042-0080 |
DOI: | 10.1155/2017/3176805 |