CRISPR therapy corrects muscular dystrophy mutations and regrows muscles in mice

CRISPR therapy corrects muscular dystrophy mutations and regrows muscles in mice

Researchers at the Experimental and Clinical Research Center (ECRC), a joint institution of the Max Delbrück Center and Charité—Universitätsmedizin Berlin, have developed a promising gene-editing approach intended to restore the function of a protein that is essential to repair and regrow muscle in patients with muscular dystrophy diseases. The findings are published in the journal Nature Communications.

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