In DMD, there is a complete absence of dystrophin in skeletal muscles and evidence of contraction‐induced muscle injury from early life, leading to muscle degeneration and functional deterioration, which constitutes a fundamental phenotype of DMD (Burns et al., 2018; Burns, Drummond et al., 2019; Burns, Murphy et al., 2019; O'Halloran et al., 2023). This evidence concerns the gene DMD and Duchenne muscular dystrophy.