Gene-Editing Alternative Corrects Duchenne Muscular Dystrophy – Drug Discovery & Development
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Gene-Editing Alternative Corrects Duchenne Muscular Dystrophy
Drug Discovery & Development Using the new gene-editing enzyme CRISPR–Cpf1, researchers at UT Southwestern Medical Center have successfully corrected Duchenne muscular dystrophy in human cells and mice in the lab. The UT Southwestern group had previously used … A New Flavor of CRISPR Could Tackle Some of the Worst Genetic Diseases CRISPR Corrects Duchenne-Causing Mutations Accurate DNA misspelling correction method |
