A nonhuman primate model of inherited retinal disease

Inherited retinal degenerations are a common cause of untreatable blindness worldwide, with retinitis pigmentosa and cone dystrophy affecting approximately 1 in 3500 and 1 in 10,000 individuals, respectively. A major limitation to the development of effective therapies is the lack of availability of...

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Detalles Bibliográficos
Autores principales: Moshiri, Ala, Chen, Rui, Kim, Soohyun, Harris, R. Alan, Li, Yumei, Raveendran, Muthuswamy, Davis, Sarah, Liang, Qingnan, Pomerantz, Ori, Wang, Jun, Garzel, Laura, Cameron, Ashley, Yiu, Glenn, Stout, J. Timothy, Huang, Yijun, Murphy, Christopher J., Roberts, Jeffrey, Gopalakrishna, Kota N., Boyd, Kimberly, Artemyev, Nikolai O., Rogers, Jeffrey, Thomasy, Sara M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Clinical Investigation 2019
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6355306/
https://www.ncbi.nlm.nih.gov/pubmed/30667376
http://dx.doi.org/10.1172/JCI123980

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6355306/
https://www.ncbi.nlm.nih.gov/pubmed/30667376
http://dx.doi.org/10.1172/JCI123980

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