-
Study on Mice Suggests Gene Therapy May Treat DMD Long-Term
A single administration of CRISPR-Cas9 gene therapy may successfully treat Duchenne muscular dystrophy in the long term, a study in mice shows. Click here to learn more.
Are you optimistic about this gene therapy’s potential for treating DMD? Why or why not?
Sorry, there were no replies found.
Log in to reply.