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Methods of diagnosing risk of myocardial infarction by detection of polymorphisms in connexin and NADH/NADPH oxidase genes

机译:通过检测连接蛋白和NADH / NADPH氧化酶基因多态性诊断心肌梗塞风险的方法

摘要

It is intended to provide a means of diagnosing myocardial infarction which shows a high accuracy and a high predictability. The risk of myocardial infarction is diagnosed by a method comprising the following steps: (i) the step of analyzing 2 or more polymorphisms among 10 gene polymorphisms or 5 gene polymorphisms proved as relating to myocardial infarction; (ii) the step of determining the genotype of a nucleic acid sample based on the polymorphism data obtained in the above step; and (iii) the step of determining the genetic risk of myocardial infarction from the genotype thus obtained.
机译:旨在提供一种诊断心肌梗塞的方法,该方法显示出高精度和高可预测性。通过包括以下步骤的方法来诊断心肌梗塞的风险:(i)分析证实与心肌梗塞有关的10个基因多态性或5个基因多态性中的2个或多个多态性的步骤; (ii)基于在上述步骤中获得的多态性数据来确定核酸样品的基因型的步骤; (iii)根据由此获得的基因型确定心肌梗塞的遗传风险的步骤。

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