CRISPR-Gold corrects gene mutations in mice with Duchenne muscular dystrophy

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Scientists at the University of California, Berkeley, have engineered a new way to deliver CRISPR-Cas9 gene-editing technology inside cells and have demonstrated in mice that the technology can repair the mutation that causes Duchenne muscular dystrophy, a severe muscle-wasting disease.

Source: http://www.news-medical.net

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