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Cathepsin D gene exon 2 polymorphism and sporadic Alzheimer's disease.

机译:组织蛋白酶D基因外显子2多态性与偶发性阿尔茨海默氏病。

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摘要

It has recently been reported that a genetic polymorphism in exon 2 of the cathepsin D gene conferred increased risk for development of Alzheimer's disease (AD). Because of the potential importance of this report we tested this association in a clinically well-defined group of AD patients and age and sex matched control subjects from the relatively genetically homogeneous Northern Ireland population. This study failed to confirm the reported association between the cathepsin D exon 2 polymorphism and AD. We conclude that if an association exists between this polymorphism and AD it is likely to be small.
机译:最近有报道说,组织蛋白酶D基因第2外显子的遗传多态性增加了患阿尔茨海默氏病(AD)的风险。由于本报告的潜在重要性,我们在临床上明确定义的一组AD患者以及年龄和性别相匹配的对照组中,从相对遗传均匀的北爱尔兰人群中测试了这种关联。这项研究未能证实组织蛋白酶D外显子2多态性与AD之间的相关报道。我们得出的结论是,如果这种多态性与AD之间存在关联,则它可能很小。

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