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


Autoria(s): Mellick, GD; Buchanan, DD; Hattori, N; Brookes, AJ; Mizuno, Y; Le Couteur, DG; Silburn, PA
Contribuinte(s)

Donald B. Calne

Data(s)

01/01/2001

Resumo

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. <(c)> 2001 Elsevier Science Ltd. All rights reserved.

Identificador

http://espace.library.uq.edu.au/view/UQ:58720

Idioma(s)

eng

Publicador

Pergamon

Palavras-Chave #Clinical Neurology #Parkin Gene #Polymorphism #A Allele #Recessive Juvenile Parkinsonism #Homozygous Deletions #Mutations #Japanese #Families #Dna #C1 #321013 Neurology and Neuromuscular Diseases #730104 Nervous system and disorders
Tipo

Journal Article