CRISPR Gene Editing Shows Promise for Treating a Fatal Muscle Disease

Thursday, August 30, 2018 - 13:30 in Health & Medicine

Results from a dog trial may help push new Duchenne muscular dystrophy therapy toward human trials -- Read more on

Read the whole article on Scientific American

More from Scientific American

Latest Science Newsletter

Get the latest and most popular science news articles of the week in your Inbox! It's free!

Check out our next project, Biology.Net