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DRD4 and DAT1 VNTR Genotyping in Children with Attention Deficit Hyperactivity Disorder

机译:注意缺陷多动障碍儿童的DRD4和DAT1 VNTR基因分型

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摘要

The dopamine receptor-D4 and the dopamine transporter have been investigated for their role in attention deficit hyperactivity disorder (ADHD) in children. Reports of their genetic association with ADHD have shown mixed results. The aim of the study was to evaluate the association of variable number tandem repeats (VNTRs) of the DRD4 and DAT1 genes with ADHD in children. A pilot 1:1 case control study, with 44 clinically confirmed ADHD cases and 44 age/gender matched healthy controls, was conducted at a tertiary care centre in Mumbai. Variable number tandem repeats of DRD4 exon 3, DAT1 intron 8 and 3′UTR were genotyped by PCR-AGE. Several allele repeats of the genes were observed in the screened subjects. Statistical significance was observed for the 10R/10R genotype of the DAT1 3′UTR VNTR between cases and controls.
机译:已经研究了多巴胺受体D4和多巴胺转运蛋白在儿童注意缺陷多动障碍(ADHD)中的作用。他们与多动症的遗传关联的报告显示出好坏参半。这项研究的目的是评估DRD4和DAT1基因的可变数目串联重复序列(VNTR)与儿童多动症的关系。在孟买一家三级医疗中心进行了一项1:1病例对照试验,研究对象包括44例临床确诊的ADHD病例和44例年龄/性别相匹配的健康对照者。通过PCR-AGE对DRD4外显子3,DAT1内含子8和3'UTR的可变数目的串联重复序列进行基因分型。在筛选的受试者中观察到基因的几个等位基因重复。在病例与对照之间观察到DAT1 3'UTR VNTR的10R / 10R基因型具有统计学意义。

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