DNM2 and autosomal dominant centronuclear myopathy: Mutations in the DNM2 gene cause two autosomal dominant motor disorders, centronuclear myopathy (CNM) (Bitoun et al., 2005) and Charcot-Marie-Tooth disease (CMT) (Züchner et al., 2005), which affect muscle and nerve, respectively (Zhao et al., 2018).