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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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| Pubblicato in: | Prog Retin Eye Res |
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| Autori principali: | , , , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
2017
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| Soggetti: | |
| Accesso online: | 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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