Furthermore, the list contained genes for which we had identified single T-ALL cases with a somatic mutation in our previous exome study: ANKRD11, CTCF, DOCK2, H3F3A, and HADHA. We did not select these genes before in our Exome-seq cohort [17] because they were only mutated in one of the 39 samples we analyzed. The gene discussed is HADHA; the disease is acute lymphoblastic leukemia.