Rod function deficit in retained photoreceptors of patients with class B Rhodopsin mutations

A common inherited retinal disease is caused by mutations in RHO expressed in rod photoreceptors that provide vision in dim ambient light. Approximately half of all RHO mutations result in a Class B phenotype where mutant rods are retained in some retinal regions but show severe degeneration in othe...

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Detalles Bibliográficos
Autores principales: Cideciyan, Artur V., Jacobson, Samuel G., Roman, Alejandro J., Sumaroka, Alexander, Wu, Vivian, Charng, Jason, Lisi, Brianna, Swider, Malgorzata, Aguirre, Gustavo D., Beltran, William A.
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/PMC7387454/
https://www.ncbi.nlm.nih.gov/pubmed/32724127
http://dx.doi.org/10.1038/s41598-020-69456-3

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7387454/
https://www.ncbi.nlm.nih.gov/pubmed/32724127
http://dx.doi.org/10.1038/s41598-020-69456-3

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