Promising Therapeutic Approaches Using CRISPR / Cas9 Genome Editing Technology in the Treatment of Duchenne Muscular Dystrophy
In this study, we briefly explained the molecular genetics of DMD and a historical overview of DMD gene therapy. We in particular focused on CRISPR/Cas9-mediated therapeutic approaches that used to treat DMD.
Source: Genes and Diseases - Category: Genetics & Stem Cells Source Type: research
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