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Inherent Instability of the Retinitis Pigmentosa P23H Mutant Opsin
The P23H opsin mutation is the most common cause of autosomal dominant retinitis pigmentosa. Even though the pathobiology of the resulting retinal degeneration has been characterized in several animal models, its complex molecular mechanism is not well understood. Here, we expressed P23H bovine rod...
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| Main Authors: | , , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
American Society for Biochemistry and Molecular Biology
2014
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3979360/ https://ncbi.nlm.nih.gov/pubmed/24515108 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1074/jbc.M114.551713 |
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