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  CRISPR-Cas9 Corrects DMD-causing Mutation in Mice and Human Cells

  Posted by MD forums Moderator on March 26, 2019 at 8:33 am

  Click here to read about how researchers used CRISPR-Cas9 to restore a functional dystrophin gene to correct a common mutation behind Duchenne muscular dystrophy (DMD).

  What are your thoughts on this news?

  MD forums Moderator replied 5 years, 1 month ago 1 Member · 0 Replies
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