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Method for providing the information for predicting or diagnosing of atrial fibrillation using single nucleotide polymorphism

机译:使用单核苷酸多态性提供用于预测或诊断心房颤动的信息的方法

摘要

The present invention relates to a method for providing information on the prediction or diagnosis of atrial fibrillation by identifying a single nucleotide polymorphism in a locus of a locus. The method of providing information of the present invention is a method for detecting a single nucleotide polymorphism associated with atrial fibrillation diagnosis and prediction, In addition to confirming using the genome association analysis method, we have confirmed the first Korean specific single nucleotide polymorphism, so that it can be used as personalized information in various treatment processes such as treatment, The risk of atrial fibrillation can be effectively used to reduce the risk of atrial fibrillation because it can provide a basis for preventive and active intervention for the increase of atrial fibrillation with increasing age.
机译:本发明涉及通过鉴定基因座中的一个位点的单核苷酸多态性来提供有关心房颤动的预测或诊断的信息的方法。本发明的提供信息的方法是一种检测与心房颤动诊断和预测有关的单核苷酸多态性的方法,除了使用基因组关联分析方法进行确认以外,我们还确认了第一个韩国特异性单核苷酸多态性,因此它可以在各种治疗过程(例如治疗)中用作个性化信息。房颤的风险可以有效地用于降低房颤的风险,因为它可以为预防和积极干预提供基础,以增加房颤的发生年龄。

著录项

  • 公开/公告号KR101883657B1

    专利类型

  • 公开/公告日2018-07-31

    原文格式PDF

  • 申请/专利权人 연세대학교 산학협력단;

    申请/专利号KR20160058906

  • 发明设计人 박희남;이지영;

    申请日2016-05-13

  • 分类号C12Q1/68;

  • 国家 KR

  • 入库时间 2022-08-21 12:37:24

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