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Method for diagnosing an increased risk for thrombosis or a genetic defect causing thrombosis and kit for use with the same
Method for diagnosing an increased risk for thrombosis or a genetic defect causing thrombosis and kit for use with the same
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机译:诊断血栓形成或引起血栓形成的遗传缺陷的风险增加的方法和与之配套的试剂盒
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摘要
Method for screening for the presence of a genetic defect associated with thrombosis and/or poor anticoagulant response to activated protein C (APC). The method is directed at detecting one or more mutations at one or more of the cleavage and/or binding sites for APC of Factor V and/or Factor Va or at Factor VIII and/or Factor VIIIa at either nucleic acid or protein level or both.
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