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Mutation analysis of DJ-1 in patients with early-onset Parkinson’s disease and relationship between the g. 168185del polymorphism and Parkinson’s disease

机译:帕金森氏病早期发作患者DJ-1突变分析及其与g的关系。 168 1 85del多态性与帕金森氏病

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摘要

Objective To evaluate the prevalence of the DJ-1mutation in early-onset Parkinson’s disease (EOPD) patients,and analyzed the association between the certain polymorphic marker g.168185del in intron 1 and Parkinson’s disease (PD) .Methods We screened all 7exons and exon-intron boundary regions of DJ-1 by PCR and direct nucleotide sequencing in 90 Chinese patients with EOPD.We also compared the allele and genotype frequencies of the g.168185del polymorphism between
机译:目的评估早发性帕金森病(EOPD)患者DJ-1突变的患病率,并分析内含子1中某些多态性标志物g.168 1 85del与帕金森病(PD)的相关性方法:对90例中国EOPD患者进行PCR和直接核苷酸测序,筛选出DJ-1的7个外显子和内含子-内含子边界区域,并对g.168 1 85del之间的多态性

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