...
机译:载脂蛋白A5基因C56G变异赋予大血管相关性缺血性卒中发展风险
University of Pécs Dept. of Medical Genetics and Child Development Szigeti 12 7624 Pécs Hungary;
University of Pécs Dept. of Medical Genetics and Child Development Szigeti 12 7624 Pécs Hungary;
Dept. of Cerebrovascular Diseases Pándy Kálmán County Hospital Gyula Hungary;
Central Laboratory Markusovszky County Hospital Szombathely Hungary;
University of Pécs Dept. of Medical Genetics and Child Development Szigeti 12 7624 Pécs Hungary;
APOA5; C56G (S19W); ischemic stroke; susceptibility; IMT;
机译:载脂蛋白A5基因C56G变异赋予大血管相关性缺血性卒中发展风险。
机译:载脂蛋白A5基因IVS3 + G476A A Helic变异赋予缺血性中风发展的敏感性
机译:载脂蛋白A5基因启动子区域T-1131C多态性与循环甘油三酸酯水平升高相关,并赋予缺血性中风发展的敏感性。
机译:中国青年人内皮型一氧化氮合酶基因多态性与缺血性卒中的风险
机译:血小板功能的遗传变异是缺血性卒中的危险因素。
机译:大血管缺血性卒中患者P2RY1–P2RY12嘌呤能受体基因编码区有害稀有变异的特定人群关联
机译:载脂蛋白A5基因IVS3 + G476A等位基因变异赋予缺血性卒中发育的易感性