Object:To detect the factor X gene mutation in one pedigree with the congenital factor X deficiency. Materials and Methods:PT、APTT and FX:C were texted for diagnosis of phenotype.
目的:对一个凝血因子X(FX))缺陷症家系进行FX基因突变的检测。
参考来源 - 一个家系中一种新的突变Val(GTC)384Ala(GCC)导致遗传性凝血因子X缺乏症的研究·2,447,543篇论文数据,部分数据来源于NoteExpress
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