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The molecular and cellular basis of rhodopsin retinitis pigmentosa reveals potential strategies for therapy
Inherited mutations in the rod visual pigment, rhodopsin, cause the degenerative blinding condition, retinitis pigmentosa (RP). Over 150 different mutations in rhodopsin have been identified and, collectively, they are the most common cause of autosomal dominant RP (adRP). Mutations in rhodopsin are...
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| Publicado no: | Prog Retin Eye Res |
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| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2017
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5779616/ https://ncbi.nlm.nih.gov/pubmed/29042326 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.preteyeres.2017.10.002 |
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