Cargando…
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...
| Autores principales: | , , , , , , , , , |
|---|---|
| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Nature Publishing Group UK
2020
|
| Materias: | |
| 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 |