| BBC News | Gene editing treats disease in mice BBC News Researchers in the US have used gene editing to treat mice with Duchenne muscular dystrophy. A team at Duke University used a system known as CRISPR-Cas9 to delete DNA that was preventing cells from producing a protein essential for muscle function. Gene Editing Offers Hope for Treating Duchenne Muscular Dystrophy, Studies Find Scientists stop Duchenne muscular dystrophy with gene editing Gene- editing could treat muscular dystrophy |
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