https://medlineplus.gov/genetics/condition/leber-congenital-amaurosis/
Leber congenital amaurosis: MedlinePlus Genetics
Leber congenital amaurosis, also known as LCA, is an eye disorder that is present from birth. Explore symptoms, inheritance, genetics of this condition.
leber congenital amaurosismedlineplusgenetics
https://pubmed.ncbi.nlm.nih.gov/22842229/
Mutations in NMNAT1 cause Leber congenital amaurosis with early-onset severe macular and optic...
In addition to its activity in nicotinamide adenine dinucleotide (NAD(+)) synthesis, the nuclear nicotinamide mononucleotide adenyltransferase NMNAT1 acts as a...
https://www.nei.nih.gov/research-and-training/research-news/phase-1-clinical-trial-results-gene-transfer-leber-congenital-amaurosis-reported
Phase 1 Clinical Trial Results of Gene Transfer for Leber Congenital Amaurosis Reported | National...
Three young adults with Leber Congenital Amaurosis-a severe degenerative disease of the retina caused by a mutation in the RPE65 gene-reported improvements in...