Gene of the issue: RUNX1 mutations and inherited bleeding
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DOI: 10.1080/09537104.2017.1280151
Abstract: Familial platelet disorder with predisposition to acute myelogenous leukemia (FPD/AML) (OMIM #601399) is an autosomal dominant disorder characterized by quantitative and qualitative platelet defects and an increased risk of AML. FPD/AML shares phenotypic similarities with… read more here.
Keywords: runx1; fpd aml; runx1 defects; gene ... See more keywords