DNM2 and autosomal dominant centronuclear myopathy: DNM2 is mutated in different neuromuscular diseases: autosomal dominant centronuclear myopathy (CNM; MIM#160150)18,19, autosomal dominant Charcot-Marie-Tooth peripheral neuropathy (CMT; MIM#606482)20, and recessive lethal congenital contracture syndrome (MIM#615368)21.