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Inherited Membrane Disorders of Muscle: Duchenne Muscular Dystrophy and Myotonic Muscular Dystrophy

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Physiology of Membrane Disorders

Abstract

Our progress in understanding the pathogenesis of human muscular dystrophies has been extremely slow, despite the fact that the majority of such syndromes are inherited diseases, and our general progress in understanding other genetic diseases of man has moved at a rapidly accelerating pace. Such slow progress might be related primarily to our ignorance of the most appropriate biochemical approaches to these problems, but it can also be attributed to a relatively unproductive concentration of research efforts on muscle tissue which has undergone numerous secondary changes. In addition, considerable effort has been invested in experimental models of myotonia and dystrophy which bear only minimal resemblance to the human disorders.

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Roses, A.D., Appel, S.H. (1978). Inherited Membrane Disorders of Muscle: Duchenne Muscular Dystrophy and Myotonic Muscular Dystrophy. In: Andreoli, T.E., Hoffman, J.F., Fanestil, D.D. (eds) Physiology of Membrane Disorders. Springer, Boston, MA. https://doi.org/10.1007/978-1-4613-3958-8_38

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