A New Mouse Model for Complete Congenital Stationary Night Blindness Due to Gpr179 Deficiency

Mutations in GPR179 lead to autosomal recessive complete congenital stationary night blindness (cCSNB). This condition represents a signal transmission defect from the photoreceptors to the ON-bipolar cells. To confirm the phenotype, better understand the pathogenic mechanism in vivo, and provide a...

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Detalles Bibliográficos
Autores principales: Orhan, Elise, Neuillé, Marion, de Sousa Dias, Miguel, Pugliese, Thomas, Michiels, Christelle, Condroyer, Christel, Antonio, Aline, Sahel, José-Alain, Audo, Isabelle, Zeitz, Christina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8122890/
https://www.ncbi.nlm.nih.gov/pubmed/33922602
http://dx.doi.org/10.3390/ijms22094424

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8122890/
https://www.ncbi.nlm.nih.gov/pubmed/33922602
http://dx.doi.org/10.3390/ijms22094424

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