For instance, as previously reported [17], the EAA software analysis identified MBNL1 (Muscleblind-like splicing regulator 1) exon 7 inclusion (Fig. S1) and FHOD1 (Formin HOmology 2 Domain containing 1) exon 11 inclusion (Fig. S2) events as more frequent in DM2 patients compared to controls. The gene discussed is FHOD1; the disease is myotonic dystrophy type 2.