Night blindness, congenital stationary, type 1E; CSNB1E

Disease ID:690
Name:Night blindness, congenital stationary, type 1E; CSNB1E
Associated with:1 target
Synonyms
Congenital stationary night blindness
Database Links
Disease Ontology: DOID:0050534
OMIM: 614565
Orphanet: ORPHA215

Targets

GPR179
References:  1

Ligands

No ligand related data available for Night blindness, congenital stationary, type 1E; CSNB1E

References

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1. Peachey NS, Ray TA, Florijn R, Rowe LB, Sjoerdsma T, Contreras-Alcantara S, Baba K, Tosini G, Pozdeyev N, Iuvone PM et al.. (2012) GPR179 is required for depolarizing bipolar cell function and is mutated in autosomal-recessive complete congenital stationary night blindness. Am. J. Hum. Genet., 90 (2): 331-9. [PMID:22325362]