Gene Therapy with Voretigene Neparvovec Improves Vision and Partially Restores Electrophysiological Function in Pre-School Children with Leber Congenital Amaurosis
Leber congenital amaurosis caused by mutations in the RPE65 gene belongs to the most severe early-onset hereditary childhood retinopathies naturally progressing to legal blindness. The novel gene therapy voretigene neparvovec is the first approved causative treatment option for this devastating eye...
Autors principals: | , , , , , , , , , |
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Format: | Article |
Idioma: | English |
Publicat: |
MDPI AG
2022-12-01
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Col·lecció: | Biomedicines |
Matèries: | |
Accés en línia: | https://www.mdpi.com/2227-9059/11/1/103 |