Mice Lacking Gpr179 with Complete Congenital Stationary Night Blindness Are a Good Model for Myopia

Mutations in GPR179 are one of the most common causes of autosomal recessive complete congenital stationary night blindness (cCSNB). This retinal disease is characterized in patients by impaired dim and night vision, associated with other ocular symptoms, including high myopia. cCSNB is caused by a...

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Detalles Bibliográficos
Autores principales: Wilmet, Baptiste, Callebert, Jacques, Duvoisin, Robert, Goulet, Ruben, Tourain, Christophe, Michiels, Christelle, Frederiksen, Helen, Schaeffel, Frank, Marre, Olivier, Sahel, José Alain, Audo, Isabelle, Picaud, Serge, Zeitz, Christina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9820543/
https://www.ncbi.nlm.nih.gov/pubmed/36613663
http://dx.doi.org/10.3390/ijms24010219

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9820543/
https://www.ncbi.nlm.nih.gov/pubmed/36613663
http://dx.doi.org/10.3390/ijms24010219

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