The F220C and F45L rhodopsin mutations identified in retinitis pigmentosa patients do not cause pathology in mice

Retinitis pigmentosa is a retinal degenerative disease that leads to blindness through photoreceptor loss. Rhodopsin is the most frequently mutated protein in this disease. While many rhodopsin mutations have well-understood consequences that lead to cell death, the disease association of several rh...

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Detalles Bibliográficos
Autores principales: Lewis, Tylor R., Shores, Camilla R., Cady, Martha A., Hao, Ying, Arshavsky, Vadim Y., Burns, Marie E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7200662/
https://www.ncbi.nlm.nih.gov/pubmed/32371886
http://dx.doi.org/10.1038/s41598-020-64437-y

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7200662/
https://www.ncbi.nlm.nih.gov/pubmed/32371886
http://dx.doi.org/10.1038/s41598-020-64437-y

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