Transgenic Expression of Cacna1f Rescues Vision and Retinal Morphology in a Mouse Model of Congenital Stationary Night Blindness 2A (CSNB2A)

PURPOSE: Congenital stationary night blindness 2A (CSNB2A) is a genetic retinal disorder characterized by poor visual acuity, nystagmus, strabismus, and other signs of retinal dysfunction resulting from mutations in Cacna1f—the gene coding for the pore-forming subunit of the calcium channel Ca(V)1.4...

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Detalles Bibliográficos
Autores principales: Waldner, Derek M., Ito, Kenichi, Chen, Li-Li, Nguyen, Lisa, Chow, Robert L., Lee, Amy, Rancourt, Derrick E., Tremblay, Francois, Stell, William K., Bech-Hansen, N. Torben
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Association for Research in Vision and Ophthalmology 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7571326/
https://www.ncbi.nlm.nih.gov/pubmed/33117610
http://dx.doi.org/10.1167/tvst.9.11.19

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7571326/
https://www.ncbi.nlm.nih.gov/pubmed/33117610
http://dx.doi.org/10.1167/tvst.9.11.19

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