Somatic point mutations in RUNX1/CBFA2/AML1 are common in high-risk myelodysplastic syndrome, but not in myelofibrosis with myeloid metaplasia

David P. Steensma, Richard J. Gibbons, Ruben A. Mesa, Ayalew Tefferi, Douglas R. Higgs

Research output: Contribution to journal › Article › peer-review

57 Scopus citations

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