Of these, two genes, CALU and PTORPG, that were predicted as targets of the dysregulated miRNAs in both DM1 and DM2, three genes PKHD1, TBC1D25 and MRPS5, that were predicted as targets of the dysregulated miRNAs in DM1, DM2 and DMD and one gene, BCAT1, that was predicted as target of the dysregulated miRNAs in the four types of muscular dystrophies analysed, DM1, DM2, DMD and FSHD1, were previously described to be involved to the corresponding muscular dystrophies [72–74]. The gene discussed is TBC1D25; the disease is myotonic dystrophy type 1.