Rhesus macaques with an OPA1 mutation demonstrate features of autosomal dominant optic atrophy

Proceedings of the National Academy of Sciences, Volume 123, Issue 16, April 2026. <br/>SignificanceOptic neuropathies due to heritable diseases are a common cause of blindness in humans, but limited therapies currently exist for the vision loss that occurs from them. One such condition is autosomal dominant optic atrophy (ADOA), an …