The combination of NPM1, DNMT3A, and IDH1/2 mutations leads to inferior overall survival in AML
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DOI: 10.1002/ajh.25517
Abstract: Acute myeloid leukemia (AML) is a genetically heterogeneous disease with a clinical course predicted by recurrent cytogenetic abnormalities and/or gene mutations. The NPM1 insertion mutations define the largest distinct genetic subset, ∼30% of AML, and… read more here.
Keywords: dnmt3a; overall survival; npm1 dnmt3a; inferior overall ... See more keywords