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CRISPR is a powerful gene-editing technology that can target disease-causing genes, with preclinical work and early human trials pointing toward therapeutic applications. Studies described include correction of mutations associated with muscular dystrophy and other serious diseases,…

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Science Digest

CRISPR gene editing successfully stopped the progression of Duchenne muscular dystrophy in dogs. It restored muscle function in their hearts & more.

Sep 1, 2018

“CRISPR gene editing successfully stopped the progression of Duchenne muscular dystrophy in dogs. It restored muscle function in their hearts, diaphragms and other muscles. Duchenne muscular dystrophy is caused by a mutation in a gene called dystrophin, which is critical for muscle function.”

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