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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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| Publicat a: | Int J Mol Sci |
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| Autors principals: | , , , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
MDPI
2021
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8122890/ https://ncbi.nlm.nih.gov/pubmed/33922602 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/ijms22094424 |
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