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Genetic polymorphisms associated with coronary heart disease, methods of detection and uses thereof

机译:与冠心病有关的遗传多态性,检测方法和用途

摘要

The present invention is based on the discovery of genetic polymorphisms that are associated with coronary heart disease and in particular stenosis and MI and response to drug treatment. In particular, the present invention relates to nucleic acid molecules containing the polymorphisms, variant proteins encoded by such nucleic acid molecules, reagents for detecting the polymorphic nucleic acid molecules and proteins, and methods of using the nucleic acid and proteins as well as methods of using reagents for their detection.
机译:本发明基于发现与冠心病特别是狭窄和MI有关的遗传多态性以及对药物治疗的反应。特别地,本发明涉及包含多态性的核酸分子,由该核酸分子编码的变异蛋白,用于检测多态性核酸分子和蛋白质的试剂,使用该核酸和蛋白质的方法以及使用该核酸的方法。用于检测的试剂。

著录项

  • 公开/公告号EP2113572B1

    专利类型

  • 公开/公告日2012-12-05

    原文格式PDF

  • 申请/专利权人 CELERA CORP;

    申请/专利号EP20090010224

  • 申请日2006-03-13

  • 分类号C12Q1/68;

  • 国家 EP

  • 入库时间 2022-08-21 16:34:33

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