Your browser doesn't support javascript.
loading
The parkin gene S/N167 polymorphism in Australian Parkinson's disease patients and controls.
Mellick, G D.; Buchanan, D D.; Hattori, N; Brookes, A J.; Mizuno, Y; Le Couteur, D G.; Silburn, P A..
Afiliação
  • Mellick GD; Department of Medicine, University of Queensland, Princess Alexandra Hospital, Queensland, Woolloongabba, Australia
Parkinsonism Relat Disord ; 7(2): 89-91, 2001 Apr.
Article em En | MEDLINE | ID: mdl-11248588
This study determined the frequencies of a G-to-A transition (S/N167) polymorphism in exon 4 of the parkin gene in Australian Parkinson's disease patients and control subjects. The genotype of each subject was determined using the polymerase chain reaction and restriction-fragment-length-polymorphism analysis. Overall, the A allele was significantly less common in the Parkinson'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 onset Parkinson's disease group (6.6%) was not significantly different to controls. The A allele is less common in Australian Caucasian subjects compared to Japanese Parkinson's disease patients and appears to be under-represented in older-onset Parkinson's disease.
Buscar no Google
Base de dados: MEDLINE Idioma: En Revista: Parkinsonism Relat Disord Assunto da revista: NEUROLOGIA Ano de publicação: 2001 Tipo de documento: Article País de afiliação: Austrália
Buscar no Google
Base de dados: MEDLINE Idioma: En Revista: Parkinsonism Relat Disord Assunto da revista: NEUROLOGIA Ano de publicação: 2001 Tipo de documento: Article País de afiliação: Austrália