Targeting of exon VI-skipping human RGR-opsin to the plasma membrane of pigment epithelium and co-localization with terminal complement complex C5b-9

PURPOSE: Rare mutations in the human RGR gene lead to autosomal recessive retinitis pigmentosa or dominantly inherited peripapillary choroidal atrophy. Here, we analyze a common exon-skipping isoform of the human retinal G protein-coupled receptor opsin (RGR-d) to determine differences in subcellula...

Descripción completa

Detalles Bibliográficos
Autores principales: Kochounian, Harold, Zhang, Zhaoxia, Spee, Christine, Hinton, David R., Fong, Henry K. W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Vision 2016
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4783578/
https://www.ncbi.nlm.nih.gov/pubmed/27011730

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4783578/
https://www.ncbi.nlm.nih.gov/pubmed/27011730

Ejemplares similares