The mutations in patients with factor V deficiency were identified including point mutation, frameshift mutation, deletion and insertion mutation.
本课题在对具有先天性出血倾向的门诊患者进行筛查的过程中，发现了一例重型凝血因子V缺乏症患者。
Objective To develope a western blot of human plasma factor V (FV) and conduct immunoblot analyses on riasma FV from a family with hereditary FV deficiency.
目的建立人血浆因子V（FV）蛋白免疫印迹分析，对遗传性FV缺乏症家系成员血浆FV含量进行分析。
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