Photoreceptor Disc Enclosure Occurs in the Absence of Normal Peripherin-2/rds Oligomerization

Mutations in the peripherin-2 gene (PRPH2, also known as rds) cause a heterogeneous range of autosomal dominant retinal diseases. PRPH2 encodes a photoreceptor-specific tetraspanin protein, PRPH2, that is a main structural component of the photoreceptor outer segment. PRPH2 distributes to the rims o...

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Detalles Bibliográficos
Autores principales: Lewis, Tylor R., Makia, Mustafa S., Kakakhel, Mashal, Al-Ubaidi, Muayyad R., Arshavsky, Vadim Y., Naash, Muna I.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Cellular Neuroscience
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7198881/
https://www.ncbi.nlm.nih.gov/pubmed/32410962
http://dx.doi.org/10.3389/fncel.2020.00092

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7198881/
https://www.ncbi.nlm.nih.gov/pubmed/32410962
http://dx.doi.org/10.3389/fncel.2020.00092

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