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Genetic analysis of DJ-1 in a cohort Parkinson's disease patients of different ethnicity.

机译:不同种族的队列帕金森氏病患者DJ-1的遗传分析。

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摘要

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.
机译:DJ-1基因的突变已在欧洲血统的常染色体隐性隐性帕金森氏病患者(ARPD)和年轻发病(YOPD)的Ashkenazi犹太裔和非洲加勒比海患者中进行了描述。关于亚洲PD人群中DJ-1突变患病率的信息很少。在这项研究中,我们在三级转诊中心的多族裔PD患者(中国人,马来人和印度人)中检查了连续YOPD和ARPD中DJ-1突变。进行了所有外显子以及DJ-1基因的外显子和内含子边界的序列分析。在这些患者中我们没有发现任何DJ-1突变。检测到许多基因型频率为15%至90%的内含子变体。与帕金病不同,致病性DJ-1突变似乎仅限于某些人群,在我们的亚洲人群中不太可能具有临床重要性。

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