As we know, most heterozygous DMD mutations’ female carriers were asymptomatic, however, although of which 2.5–7.8% were symptomatic with symptoms ranging from mild muscle weakness to a rapidly progressive DMD-like MD (Moser and Emery, 1974; Norman and Harper, 1989; Taylor et al., 2007). Here, DMD is linked to Duchenne muscular dystrophy.