Haematologica (Feb 2014)

Rare coincident NPM1 and RUNX1 mutations in intermediate risk acute myeloid leukemia display similar patterns to single mutated cases

  • Annette Fasan,
  • Claudia Haferlach,
  • Alexander Kohlmann,
  • Frank Dicker,
  • Christiane Eder,
  • Wolfgang Kern,
  • Torsten Haferlach,
  • Susanne Schnittger

DOI
https://doi.org/10.3324/haematol.2013.099754
Journal volume & issue
Vol. 99, no. 2

Abstract

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