Rpgrip1 is required for rod outer segment development and ciliary protein trafficking in zebrafish

Mutations in the RPGR-interacting protein 1 (RPGRIP1) gene cause recessive Leber congenital amaurosis (LCA), juvenile retinitis pigmentosa (RP) and cone-rod dystrophy. RPGRIP1 interacts with other retinal disease-causing proteins and has been proposed to have a role in ciliary protein transport; how...

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Detalles Bibliográficos
Autores principales: Raghupathy, Rakesh K., Zhang, Xun, Liu, Fei, Alhasani, Reem H., Biswas, Lincoln, Akhtar, Saeed, Pan, Luyuan, Moens, Cecilia B., Li, Wenchang, Liu, Mugen, Kennedy, Breandan N., Shu, Xinhua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5715152/
https://www.ncbi.nlm.nih.gov/pubmed/29203866
http://dx.doi.org/10.1038/s41598-017-12838-x

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