1.
Annette Fasan, Claudia Haferlach, Alexander Kohlmann, Frank Dicker, Christiane Eder, Wolfgang Kern, Torsten Haferlach, Susanne Schnittger. Rare coincident NPM1 and RUNX1 mutations in intermediate risk acute myeloid leukemia display similar patterns to single mutated cases. haematol [Internet]. 2014Feb.4 [cited 2024Nov.22];99(2):e20-e21. Available from: https://haematologica.org/article/view/6948