Mutation detection and inhibitor risk in Iranian patients with Hemophilia A: Six novel mutations

伊朗A型血友病患者的突变检测和抑制剂风险:六个新的突变

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Abstract

This investigation facilitates a better understanding of inhibitor development, the critical treatment morbidity in HA patients. Furthermore, six novel mutations are reported, which would expand the mutation spectrum of the F8 gene.

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