A Novel GATA2 Splice-Site Mutation Associated with Familial Myelodysplastic Syndrome
{{output}}
Introduction:GATA binding protein 2 (GATA2) deficiency is an autosomal dominant disorder characterized by immunodeficiency, progressive cytopenias, and an increased risk of myelodysplastic syndrome (MDS) and acute myeloid leukemia (AML). Novel variants continu... ...
