Retinal structure in Leber's congenital amaurosis caused by RPGRIP1 mutations | Human Genome Variation
Leber congenital amaurosis: MedlinePlus Genetics
FDA-approved drug shows promise in lab models for blinding childhood disease | National Institutes of Health (NIH)
Identification and Correction of Mechanisms Underlying Inherited Blindness in Human iPSC-Derived Optic Cups - ScienceDirect
JCI - Spotlight on childhood blindness
Identified the NMNAT1 mutations as a cause of Leber congenital amaurosis ( LCA), one of the most common causes of inherited blindness in children | Scientific Earth Conscientious
Gene therapy helps blindness | CTV News
What Is Leber Congenital Amaurosis (LCA)?
IJMS | Free Full-Text | Genetic and Clinical Profile of Retinopathies Due to Disease-Causing Variants in Leber Congenital Amaurosis (LCA)-Associated Genes in a Large German Cohort
LCA | Vail Ranch Pharmacy, Taking Care of People First
Leber congenital amaurosis: MedlinePlus Genetics
Leber Congenital Amaurosis (LCA): for patients - Gene Vision
Florida Boy Begins Gene Therapy This Week To Reverse His Blindness
Investigational drug gives sight to patient with inherited form of blindness - Drug Discovery and Development
FDA panel approves gene therapy to treat form of blindness | Carver College of Medicine
Fish eyes to help understand human inherited blindness