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The document reviews new therapies for Duchenne muscular dystrophy (DMD), highlighting the challenges and prospects of drug, gene, and cell therapies currently in clinical trials. It discusses the limitations of these strategies, including issues with gene delivery and the need for systemic administration to achieve clinical benefits. The review also outlines various experimental approaches and ongoing trials aimed at addressing the complexities of muscular dystrophies and improving patient outcomes.

Author

kesraunalli

Language

EN