A genetic mutation that leads to a rare, but devastating blindness-causing condition called Bardet-Biedl Syndrome has been discovered in monkeys for the first time. The finding offers a promising way to develop gene and cell therapies that could treat people with the condition, which leads to vision loss, kidney disfunction, extra fingers or toes, and other symptoms.
from Latest Science News -- ScienceDaily https://ift.tt/2WqCuzf
via IFTTT
Saturday, October 26, 2019
Discovery in monkeys could lead to treatment for blindness-causing syndrome
Subscribe to:
Post Comments (Atom)
No comments:
Post a Comment