CRISPR-Cpf1 Corrects Duchenne Mutations, Restores Dystrophin Expression, UT Study Shows – Muscular Dystrophy News
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CRISPR–Cpf1 Corrects Duchenne Mutations, Restores Dystrophin Expression, UT Study Shows
Muscular Dystrophy News Researchers from the University of Texas Southwestern Medical Center in Dallas have corrected Duchenne muscular dystrophy (DMD) mutations in human cells and experimental animal models using a new genome editing method called CRISPR–Cpf1. |
