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Congenital stationary night blindness
- Autosomal recessive congenital stationary night blindness is a disorder of the retina, which is the specialized tissue at the back of the eye that detects light ...
- Autosomal dominant congenital stationary night blindness is a disorder of the retina, which is the specialized tissue at the back of the eye that detects light ...
- X-linked congenital stationary night blindness is a disorder of the retina, which is a specialized tissue at the back of the eye that detects light and ...
- ... have been identified in people with X-linked congenital stationary night blindness. NYX gene variants are responsible for the complete ... which impairs vision in people with X-linked congenital stationary night blindness. The rod pathway is severely disrupted, while the ...
- ... have been identified in people with X-linked congenital stationary night blindness. CACNA1F gene variants are responsible for the incomplete ... which impairs vision in people with X-linked congenital stationary night blindness. More About This Health Condition MedlinePlus Genetics provides ...
- ... gene have been found to cause autosomal recessive congenital stationary night blindness, which is characterized by the inability to see ... is mutated in patients with autosomal-recessive complete congenital stationary night blindness. Am J Hum Genet. 2009 Nov;85(5): ...
- ... gene have been found to cause autosomal recessive congenital stationary night blindness, which is characterized by the inability to see ... coupling in an mGluR6 point mutant associated with congenital stationary night blindness. Mol Pharmacol. 2009 Nov;76(5):992-7. ...
- ... gene have been found to cause autosomal dominant congenital stationary night blindness, which is characterized by a loss of vision ... time. Unlike retinitis pigmentosa (described below), autosomal dominant congenital stationary night blindness does not affect daytime vision.The RHO gene ...
- ... gene have been found to cause autosomal dominant congenital stationary night blindness, which is characterized by the inability to see ... of rod transducin in the Nougaret form of congenital stationary night blindness. Nat Genet. 1996 Jul;13(3):358-60. ...
- ... gene has been found to cause autosomal dominant congenital stationary night blindness, which is characterized by the inability to see ... Artemyev NO. Mutation in rod PDE6 linked to congenital stationary night blindness impairs the enzyme inhibition by its gamma-subunit. ...
