Relative preservation of the extramacular retina in LCA5-associated Leber congenital amaurosis

Leber Congenital Amaurosis caused by mutations in LCA5 (LCA5-LCA) represents one of the most severe molecular forms of inherited retinal degenerations, even within the LCA disease spectrum. A retina-wide retinal degeneration with preservation of photoreceptors limited to central retina, near the fov...

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Detalles Bibliográficos
Autores principales: O'Connor, Keli, O'Neil, Erin C., Aleman, Tomas S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8802877/
https://www.ncbi.nlm.nih.gov/pubmed/35128149
http://dx.doi.org/10.1016/j.ajoc.2022.101260

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8802877/
https://www.ncbi.nlm.nih.gov/pubmed/35128149
http://dx.doi.org/10.1016/j.ajoc.2022.101260

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