Duchenne Muscular Dystrophy (DMD) is one of the most prevalent
genetic disorders of childhood and currently stands as an incurable
condition. This authoritative guide provides a clear overview of
the latest current and experimental approaches to the treatment of
DMD and examines the clinical, genetic, and pathophysiological
aspects of the disease in the context of emerging therapeutic
modalities. The only available source on the subject, this
reference emphasizes the importance of accurate diagnosis, carrier
detection, and genetic counseling, and supplies state-of-the-art
contributions on pharmacological interventions, regenerative
medicine, and gene therapy.
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