In experiments with rats, pigs and monkeys, researchers have developed a way to deliver sight-saving gene therapy to the retina. If proved safe and effective in humans, the technique could provide a new, more permanent therapeutic option for patients with common diseases such as wet age-related macular degeneration (AMD), and it could potentially replace defective genes in patients with inherited retinal disease.
from Latest Science News -- ScienceDaily https://ift.tt/2oBLc0z
via IFTTT
Monday, September 30, 2019
Researchers advance search for safer, easier way to deliver vision-saving gene therapy
Subscribe to:
Post Comments (Atom)
No comments:
Post a Comment