-
Study Says Gene Therapy Could Reverse Changes Related to Friedreich’s Ataxia
A gene therapy approach to deliver frataxin, the protein that’s deficient in Friedreich’s ataxia patients, was able to reverse disease-related changes, a mouse study reports. Click here to read more about about this study and its findings.
What are your thoughts on this news? Are you optimistic about the promise of gene therapies for FA?
Sorry, there were no replies found.
Log in to reply.