Disease sequence from mutant rhodopsin allele to rod and cone photoreceptor degeneration in man
Mutations in the gene encoding rhodopsin, the visual pigment in rod photoreceptors, lead to retinal degeneration in species from Drosophila to man. The pathogenic sequence from rod cell-specific mutation to degeneration of rods and cones remains unclear. To understand the disease process in man, we...
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| Publicat a: | Proc Natl Acad Sci U S A |
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| Autors principals: | , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
National Academy of Sciences
1998
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC22754/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/9618546/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.95.12.7103 |
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