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The role of the ER stress-response protein PERK in rhodopsin retinitis pigmentosa
Mutations in rhodopsin, the light-sensitive protein of rod cells, are the most common cause of dominant retinitis pigmentosa (RP), a type of inherited blindness caused by the dysfunction and death of photoreceptor cells. The P23H mutation, the most frequent single cause of RP in the USA, causes rhod...
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| Yayımlandı: | Hum Mol Genet |
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| Asıl Yazarlar: | , , , , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Oxford University Press
2017
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5868081/ https://ncbi.nlm.nih.gov/pubmed/29036441 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddx370 |
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