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
Affiliations
- Annette Fasan
- MLL Munich Leukemia Laboratory, Munich, Germany
- Claudia Haferlach
- MLL Munich Leukemia Laboratory, Munich, Germany
- Alexander Kohlmann
- MLL Munich Leukemia Laboratory, Munich, Germany
- Frank Dicker
- MLL Munich Leukemia Laboratory, Munich, Germany
- Christiane Eder
- MLL Munich Leukemia Laboratory, Munich, Germany
- Wolfgang Kern
- MLL Munich Leukemia Laboratory, Munich, Germany
- Torsten Haferlach
- MLL Munich Leukemia Laboratory, Munich, Germany
- Susanne Schnittger
- MLL Munich Leukemia Laboratory, Munich, Germany
- DOI
-
https://doi.org/10.3324/haematol.2013.099754
- Journal volume & issue
-
Vol. 99,
no. 2
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