DMD and Becker muscular dystrophy: Furthermore, two already cited DMD variants were identified: c.10,801 C > T; p.(Gln872Ter) in family B and hemizygous genomic deletion in DMD (NM_004006.3):g.32438241_32809611del (corresponding to deletion of exons 7–29; GRCh38), which was identified (in family F) associated with BMD and DMD, respectively.