NPM1 mutation but not RUNX1 mutation or multilineage dysplasia defines a prognostic subgroup within de novo acute myeloid leukemia lacking recurrent cytogenetic abnormalities in the revised 2016 WHO classification

Olga K. Weinberg, Christopher J. Gibson, Traci M. Blonquist, Donna Neuberg, Olga Pozdnyakova, Frank Kuo, Benjamin L. Ebert, Robert P. Hasserjian

Research output: Contribution to journalLetterpeer-review

8 Scopus citations
Original languageEnglish (US)
Pages (from-to)E123-E124
JournalAmerican Journal of Hematology
Volume92
Issue number7
DOIs
StatePublished - Jul 2017
Externally publishedYes

ASJC Scopus subject areas

  • Hematology

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