In detail, we found that MM and pPCL cases with t(11;14) showed a distinctive expression pattern of the BCL2 family genes (Figure 3), although, globally, both clinical entities maintained similar BCL2/BCL2L1 and BCL2/MCL1 ratios, which are parameters that have been reported to correlate with venetoclax sensitivity [27,32,38,39]. The gene discussed is BCL2L1; the disease is Miyoshi myopathy.