MM is characterized also, by specific immunoglobulin translocations, including t(11;14) (IGH-CCND1), t(4;14) (IGH-MMSET/NSD2), and t(14;16) (IGH-MAF), which lead to distinctive molecular characteristics [28,32,34,35,36,37,38,39,40]. The gene discussed is MAF; the disease is Miyoshi myopathy.