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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 the specialized tissue at the back of the eye that detects light and ...
- ... have been identified in people with X-linked congenital stationary night blindness. Mutations in this gene are responsible for the ... vision problems similar to those of X-linked congenital stationary night blindness.Researchers have identified at least one CACNA1F mutation ...
- ... have been identified in people with X-linked congenital stationary night blindness. Mutations in this gene are responsible for the ... the other vision problems characteristic of X-linked congenital stationary night blindness. The mutations responsible for high myopia each change ...
- ... 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 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. ...
- ... 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. ...
