| Literature DB >> 15308309 |
Eng-King Tan1, Chris Tan, Yi Zhao, Kenneth Yew, Hui Shen, V R Chandran, Mei-Lin Teoh, Yuan Yih, Ratnagopal Pavanni, Meng-Cheong Wong.
Abstract
Mutations in the DJ-1 gene have been described in autosomal recessive Parkinson's disease patients (ARPD) of European ancestry and young onset (YOPD) Ashkenazi Jewish and Afro-Caribbean patients. There is little information on the prevalence of DJ-1 mutations amongst Asian PD populations. In this study, we examined for DJ-1 mutations in consecutive YOPD and ARPD in a multi-ethnic cohort (Chinese, Malays, and Indians) of PD patients in a tertiary referral center. Sequence analysis of all the exons and the exon and intron boundaries of the DJ-1 gene were carried out. We did not find any DJ-1 mutations in these patients. A number of intronic variants with genotype frequency ranging from 15 to 90% were detected. Unlike Parkin, pathogenic DJ-1 mutations appear to be restricted to certain populations and are unlikely to be of clinical importance in our Asian cohort.Entities:
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Year: 2004 PMID: 15308309 DOI: 10.1016/j.neulet.2004.05.090
Source DB: PubMed Journal: Neurosci Lett ISSN: 0304-3940 Impact factor: 3.046