Researchers correct Duchenne muscular dystrophy using gene-editing alternative – News-Medical.net
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Researchers correct Duchenne muscular dystrophy using gene-editing alternative
News-Medical.net 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 … |
