The parkin gene S/N167 polymorphism in Australian Parkinson's disease patients and controls

Citation
Gd. Mellick et al., The parkin gene S/N167 polymorphism in Australian Parkinson's disease patients and controls, PARKINS R D, 7(2), 2001, pp. 89-91
Citations number
10
Categorie Soggetti
Neurology
Journal title
PARKINSONISM & RELATED DISORDERS
ISSN journal
13538020 → ACNP
Volume
7
Issue
2
Year of publication
2001
Pages
89 - 91
Database
ISI
SICI code
1353-8020(200104)7:2<89:TPGSPI>2.0.ZU;2-H
Abstract
This study determined the frequencies of a G-to-A transition (S/N167) polym orphism in exon 4 of the parkin gene in Australian Parkinson's disease pati ents and control subjects. The genotype of each subject was determined usin g the polymerase chain reaction and restriction-fragment-length-polymorphis m analysis. Overall, the A allele was significantly less common in the Park inson's disease group (1.7%) compared with the control group (3.8%, OR = 0. 43, 95% CI = 0.19-1.00, P < 0.05), although the frequency in the young onse t Parkinson's disease group (6.6%) was not significantly different to contr ols. The A allele is less common in Australian Caucasian subjects compared to Japanese Parkinson's disease patients and appears to be under-represente d in older-onset Parkinson's disease. <(c)> 2001 Elsevier Science Ltd. All rights reserved.