Curing Duchenne Muscular Dystrophy with a New Version of CRISPR – Technology Networks
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Curing Duchenne Muscular Dystrophy with a New Version of CRISPR
Technology Networks The UT Southwestern group had previously used CRISPR-Cas9, the original gene-editing system, to correct the Duchenne defect in a mouse model of the disease and in human cells. In the current work, they used a new variation of the gene-editing system to … |
