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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Detaylı Bibliyografya
Yayımlandı:Prog Retin Eye Res
Asıl Yazarlar: Athanasiou, Dimitra, Aquila, Monica, Bellingham, James, Li, Wenwen, McCulley, Caroline, Reeves, Philip J., Cheetham, Michael E.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 2017
Konular:
Article
Online Erişim: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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