CRISPR-Cas9 corrects Duchenne muscular dystrophy exon 44 deletion mutations in mice and human cells

Title
CRISPR-Cas9 corrects Duchenne muscular dystrophy exon 44 deletion mutations in mice and human cells
Authors
Keywords
-
Journal
Science Advances
Volume 5, Issue 3, Pages eaav4324
Publisher
American Association for the Advancement of Science (AAAS)
Online
2019-03-07
DOI
10.1126/sciadv.aav4324

Ask authors/readers for more resources

Find Funding. Review Successful Grants.

Explore over 25,000 new funding opportunities and over 6,000,000 successful grants.

Explore

Discover Peeref hubs

Discuss science. Find collaborators. Network.

Join a conversation