In the studied samples, the mutations in genes recurrently mutated in AML, e.g., NPM1, DNMT3A, NRAS, RUNX1, ASXL1, ATM, CEBPA seemed to play a pivotal role in leukemogenesis, whereas changes in the BCL2 family gene expression probably played a secondary role. Here, ATM is linked to acute myeloid leukemia.