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Deep dive into muscle repair yields new strategies to combat Duchenne muscular dystrophy

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Researchers at the Sanford Burnham Prebys Medical Discovery Institute (SBP) reported new findings this week that may lead to novel therapeutic strategies for people suffering from Duchenne muscular dystrophy (DMD). DMD, a muscle-wasting disease that affects 1 in 7250 males aged 5 to 24 years in the United States, is caused by a genetic mutation leading…

Frontiers Current Pharmacological Strategies for Duchenne Muscular Dystrophy

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Therapeutic approaches for Duchenne muscular dystrophy

Frontiers Duchenne muscular dystrophy: disease mechanism and therapeutic strategies

Sanford Burnham Prebys Medical Discovery Institute

Muscular Dystrophy

De novo revertant fiber formation and therapy testing in a 3D culture model of Duchenne muscular dystrophy skeletal muscle - ScienceDirect

muscle stem cells, The Stem Cellar

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Frontiers Current Pharmacological Strategies for Duchenne Muscular Dystrophy