Tuesday, February 26, 2019

More Progress Toward Gene Editing for Kids with Muscular Dystrophy

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Based on the NIH health information topics you requested to receive information about, we thought you'd be interested in this story from the NIH Director's Blog.

CRISPR-DMD

More Progress Toward Gene Editing for Kids with Muscular Dystrophy

Posted on  by Dr. Francis Collins

Thanks to CRISPR and other gene editing technologies, hopes have never been greater for treating or even curing Duchenne muscular dystrophy (DMD) and many other rare, genetic diseases that once seemed tragically out of reach. The latest encouraging news comes from a study in which a single infusion of a...

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