CRISPR Offers New Line of Attack on Muscular Dystrophy
popularmechanics.com
CRISPR Offers New Line of Attack on Muscular Dystrophy
The technique could help up to 60 percent of those suffering from a specific type of dystrophy known as DMD.
Feb 2, 2018
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Today, the Food and Drug Administration approved the first gene therapy treatment for Duchenne Muscular Dystrophy. This groundbreaking treatment, developed here at Nationwide Children’s, is giving boys like Easton and Connor a future full of hope and possibilities. Watch their incredible stories. Learn more: https://bit.ly/3PzvLQK | Nationwide Children's Hospital
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Today, the Food and Drug Administration approved the first gene therapy treatment for Duchenne Muscular Dystrophy. This groundbreaking treatment, developed here at Nationwide Children’s, is giving boys like Easton and Connor a future full of hope and possibilities. Watch their incredible stories. Learn more: https://bit.ly/3PzvLQK | Nationwide Children's Hospital
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