Kinetics of Heterogeneous Background in Stargardt’s Disease over Time

Stargardt’s disease (STGD1) is caused by mutations in the ABCA4 gene. Different lesions characterised by decreased autofluorescence levels are found in fundus autofluorescence (FAF) from STGD1 patients and could be used as outcome indicators for disease progression. We investigated the fate of foci...

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Detalles Bibliográficos
Autores principales: Rodríguez-Bocanegra, Eduardo, Biarnés, Marc, Garcia, Míriam, Ferraro, Lucía Lee, Fischer, Manuel Dominik, Monés, Jordi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8953836/
https://www.ncbi.nlm.nih.gov/pubmed/35330133
http://dx.doi.org/10.3390/life12030381

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8953836/
https://www.ncbi.nlm.nih.gov/pubmed/35330133
http://dx.doi.org/10.3390/life12030381

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