Getting a handle on hereditary CEBPA mutations

Research output: Contribution to journalComment/debatepeer-review

13 Scopus citations

Abstract

In this issue of Blood, Tawana et al describe 24 patients with acute myeloid leukemia (AML) within 10 families with germline, ie, hereditary, mutations in the CCAAT/enhancer binding protein a (CEBPA) gene. Distinct biology and clinical outcomes, including unique patterns of "relapse," are identified.

Original languageEnglish (US)
Pages (from-to)1156-1158
Number of pages3
JournalBlood
Volume126
Issue number10
DOIs
StatePublished - Sep 3 2015

ASJC Scopus subject areas

  • Biochemistry
  • Immunology
  • Hematology
  • Cell Biology

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