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Congenital stationary night blindness

Disease ID:1212
Name:Congenital stationary night blindness
Associated with:1 target
Description
Congenital stationary night blindness (CSNB) refers to a group of nonprogressive retinal disorders characterized predominantly by abnormal function of the rod system. The condition may be X-linked (the most common form), autosomal recessive, or autosomal dominant. Types 1A and 2A are X-linked.
Database Links
OMIM: 310500, 300071

Targets

regulator of G-protein signaling 11
References:  1

Ligands

No ligand related data available for Congenital stationary night blindness

References

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1. NeuillĂ© M, Morgans CW, Cao Y, Orhan E, Michiels C, Sahel JA, Audo I, Duvoisin RM, Martemyanov KA, Zeitz C. (2015) LRIT3 is essential to localize TRPM1 to the dendritic tips of depolarizing bipolar cells and may play a role in cone synapse formation. Eur. J. Neurosci., 42 (3): 1966-75. [PMID:25997951]