遗传性凝血酶原缺乏症

  • 网络hereditary prothrombin deficiency
遗传性凝血酶原缺乏症遗传性凝血酶原缺乏症
  1. 目的对1个遗传性凝血酶原缺乏症家系进行凝血酶原(FⅡ)基因突变的检测。

    Objective To investigate the gene mutations in a pedigree with inherited prothrombin ( F ⅱ) deficiency .