The lethal X-linked recessive genetic disorder Duchenne Muscular Dystrophy (DMD) affects ~one in 3500-5000 live born males; securing its status as the most frequently occurring and severe muscular dystrophy.1 It is caused by a lack of the sub-sarcolemmal protein dystrophin in skeletal and cardiac muscles where it serves to normally connect the intracellular contractile machinery to the extracellular matrix. Here, DMD is linked to Duchenne muscular dystrophy.