CRISPR halts Duchenne muscular dystrophy progression in dogs

Scientists for the first time have used CRISPR gene editing to halt the progression of Duchenne muscular dystrophy (DMD) in a large mammal, according to a new study that provides a strong indication that a lifesaving treatment may be in the pipeline.

from Health & Medicine News -- ScienceDaily https://ift.tt/2wszm9W

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