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Polymorphisms of the DAX1 and EGR4 Genes are Not Common Causes of Abnormal Spermatogenesis

机译:DAX1和EGR4基因的多态性不是精子发生异常的常见原因

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The study of gene mutations causing sequence variation in spermatogenesis-related genes has revealed a highlystable spermatogenic code with little variability and even fewer disease-causing mutations. The current study supports thesame trend, indicating that EGR4 and DAX1, two spermatogenesis-related genes, have a high genetic fidelity and do notcontain polymorphic sites that would lead to a disease state. This was determined from a population of 192 men, 96 controlsamples from men with known paternity, acquired from the Utah Genetic Reference Project (UGRP), and 96 infertilemen. The diagnosis of the infertile men was stratified amongst three diagnostic groups, non-obstructive azoospermic, severeoligozoospermic, and men with abnormal protamine expression.
机译:对引起精子发生相关基因序列变异的基因突变的研究表明,这种稳定的生精密码几乎没有变异,而致病突变则更少。当前的研究支持相同的趋势,表明与精子发生相关的两个基因EGR4和DAX1具有很高的遗传保真度,并且不包含会导致疾病状态的多态性位点。这是从192名男性,从犹他州遗传参考计划(UGRP)获得的96个已知亲权的男性的对照样本和96个不育男性中确定的。不育男性的诊断分为三个诊断组:无梗阻性无精子症,重度少精子症和鱼精蛋白表达异常的男性。

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