For children born with a rare form of inherited blindness called Leber congenital amaurosis type 16 (LCA16), the genetic culprit can be a single miswritten instruction in their DNA — a so-called “nonsense mutation” that …
Read the full article at: https://www.pediatrics.wisc.edu/a-molecular-override-for-inherited-blindness-bikash-pattnaiks-research-group-publishes-recent-paper/