Reply to "rare coincident NPM1 and RUNX1 mutations in intermediate risk acute myeloid leukemia display similar patterns to single mutated cases". Haematologica 2014;99(2):e20-21

Haematologica. 2014 Feb;99(2):e22. doi: 10.3324/haematol.2013.100669.
No abstract available

Keywords: NPM1; RUNX1; acute myeloid leukemia; germline; mutational interrelationships.

Publication types

  • Letter
  • Comment

MeSH terms

  • Core Binding Factor Alpha 2 Subunit / genetics*
  • Female
  • Germ-Line Mutation / genetics*
  • Humans
  • Leukemia, Myeloid, Acute / diagnosis*
  • Leukemia, Myeloid, Acute / genetics*
  • Male
  • Nuclear Proteins / genetics*
  • Nucleophosmin

Substances

  • Core Binding Factor Alpha 2 Subunit
  • NPM1 protein, human
  • Nuclear Proteins
  • Nucleophosmin