Factor H variants in paroxysmal nocturnal hemoglobinuria, the role of factor XII in SCD-related thrombosis, and clinical features of therapy-related NPM1-mutated AML
Blood Podcast
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Introduction
Learn how rare germline genetic variants in complement factor H, C F H, affect the course of paroxysmal nocturnal hemoglobin area. Discuss the role of coagulation factor 12 in thrombotic complications and vaso-aclusion associated with sickle cell disease. Learn more about the overlapping features of therapy-related and de novo NPM1 mutated AML.
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