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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Pubblicato in:J Neurosci
Autori principali: Lewis, Tylor R., Makia, Mustafa S., Castillo, Carson M., Al-Ubaidi, Muayyad R., Naash, Muna I., Arshavsky, Vadim Y.
Natura: Artigo
Lingua:Inglês
Pubblicazione: Society for Neuroscience 2021
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Research Articles
Accesso online: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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