A new gene therapy for Duchenne muscular dystrophy (DMD) has shown promise in not only slowing the progression of the disease but potentially even reversing the muscle damage, with human trials set to begin within two years.Continue ReadingCategory: Medical, ScienceTags: gene therapy, Genetics, Muscular Dystrophy, Disease, University of Washington
Muscular dystrophy-reversing gene therapy: Human trials in 2 years
Posted by ArielTechGeek 280 days ago (https://newatlas.com)
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