Analysis of retinal sublayer thicknesses and rates of change in ABCA4-associated Stargardt disease

Stargardt disease, the most common inherited macular dystrophy, is characterized by vision loss due to central retinal atrophy. Although clinical trials for Stargardt are currently underway, the disease is typically slowly progressive, and objective, imaging-based biomarkers are critically needed. I...

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Detalles Bibliográficos
Autores principales: Whitmore, S. Scott, Fortenbach, Christopher R., Cheng, Justine L., DeLuca, Adam P., Critser, D. Brice, Geary, Elizabeth L., Hoffmann, Jeremy M., Stone, Edwin M., Han, Ian C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7538899/
https://www.ncbi.nlm.nih.gov/pubmed/33024232
http://dx.doi.org/10.1038/s41598-020-73645-5

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7538899/
https://www.ncbi.nlm.nih.gov/pubmed/33024232
http://dx.doi.org/10.1038/s41598-020-73645-5

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