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Photoreceptor Disc Enclosure Is Tightly Controlled by Peripherin-2 Oligomerization
Mutations in the PRPH2 gene encoding the photoreceptor-specific protein PRPH2 (also known as peripherin-2 or rds) cause a broad range of autosomal dominant retinal diseases. Most of these mutations affect the structure of the light-sensitive photoreceptor outer segment, which is composed of a stack...
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| Publié dans: | J Neurosci |
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| Auteurs principaux: | , , , , , |
| Format: | Artigo |
| Langue: | Inglês |
| Publié: |
Society for Neuroscience
2021
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| Sujets: | |
| Accès en ligne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8055076/ https://ncbi.nlm.nih.gov/pubmed/33707293 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1523/JNEUROSCI.0041-21.2021 |
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