CRISPR Gene Editing Successfully Stops Muscular Dystrophy In Living Mice

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If used on humans, the treatment could save hundreds of lives per yearHundreds of children per year are born with Duchenne muscular dystrophy (DMD), a genetic disorder that leads to muscle weakness and atrophy—those numbers make it the most common fatal genetic disorder. Better care for the heart an”¦

Sursa: CRISPR Gene Editing Successfully Stops Muscular Dystrophy In Living Mice

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