Central Visual Function and Genotype–Phenotype Correlations in PDE6A-Associated Retinitis Pigmentosa

PURPOSE: Autosomal recessive retinitis pigmentosa (arRP) can be caused by mutations in the phosphodiesterase 6A (PDE6A) gene. Here, we describe the natural course of disease progression with respect to central retinal function (i.e., visual acuity, contrast sensitivity, and color vision) and establi...

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Detalles Bibliográficos
Autores principales: Kuehlewein, Laura, Straßer, Torsten, Blumenstock, Gunnar, Stingl, Katarina, Fischer, M. Dominik, Wilhelm, Barbara, Zrenner, Eberhart, Wissinger, Bernd, Kohl, Susanne, Weisschuh, Nicole, Zobor, Ditta
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Association for Research in Vision and Ophthalmology 2022
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9106976/
https://www.ncbi.nlm.nih.gov/pubmed/35533076
http://dx.doi.org/10.1167/iovs.63.5.9

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9106976/
https://www.ncbi.nlm.nih.gov/pubmed/35533076
http://dx.doi.org/10.1167/iovs.63.5.9

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