A Mild Form of RPE65-Associated Retinopathy
Author:
Affiliation:
1. University Eye Hospital Bonn, Germany
2. Department of Ophthalmology, University Hospital Essen, Germany
Publisher
Georg Thieme Verlag KG
Link
http://www.thieme-connect.de/products/ejournals/pdf/10.1055/a-2280-1536.pdf
Reference5 articles.
1. Early-onset severe rod-cone dystrophy in young children with RPE65 mutations;B Lorenz;Invest Ophthalmol Vis Sci,2000
2. The Natural History of Inherited Retinal Dystrophy Due to Biallelic Mutations in the RPE65 Gene;D C Chung;Am J Ophthalmol,2019
3. Durability of Voretigene Neparvovec for Biallelic RPE65-Mediated Inherited Retinal Disease: Phase 3 Results at 3 and 4 Years;A M Maguire;Ophthalmology,2021
4. Preserved visual function in retinal dystrophy due to hypomorphic RPE65 mutations;S Hull;Br J Ophthalmol,2016
5. Single Center Experience with Voretigene Neparvovec Gene Augmentation Therapy in RPE65 Mutation-Associated Inherited Retinal Degeneration in a Clinical Setting;B Lorenz;Ophthalmology,2024
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