Ablation of EYS in zebrafish causes mislocalisation of outer segment proteins, F-actin disruption and cone-rod dystrophy

Mutations in EYS are associated with autosomal recessive retinitis pigmentosa (arRP) and autosomal recessive cone-rod dystrophy (arCRD) however, the function of EYS and the molecular mechanisms of how these mutations cause retinal degeneration are still unclear. Because EYS is absent in mouse and ra...

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Detalles Bibliográficos
Autores principales: Lu, Zhaojing, Hu, Xuebin, Liu, Fei, Soares, Dinesh C., Liu, Xiliang, Yu, Shanshan, Gao, Meng, Han, Shanshan, Qin, Yayun, Li, Chang, Jiang, Tao, Luo, Daji, Guo, An-Yuan, Tang, Zhaohui, Liu, Mugen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5380955/
https://www.ncbi.nlm.nih.gov/pubmed/28378834
http://dx.doi.org/10.1038/srep46098

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5380955/
https://www.ncbi.nlm.nih.gov/pubmed/28378834
http://dx.doi.org/10.1038/srep46098

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