Technical Articles

凝血因子XI缺乏症:一种罕见的遗传性出血性疾病
Factor XI deficiency: a rare inherited bleeding disorder
发布时间 2026-08-04
This article systematically elaborates on the molecular pathological basis, genetic characteristics, clinical manifestations, and diagnostic and therapeutic strategies of coagulation factor XI deficiency (hemophilia C), analyzing its key differences from hemophilia A/B.
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  • Metabolism
  • Coagulation Factor XI (FXI) Protein
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