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Results 1 - 6 of 6 for Congenital stationary night blindness autosomal dominant 1
  1. ... NIGHT BLINDNESS, CONGENITAL STATIONARY, AUTOSOMAL DOMINANT 3; CSNBAD3 NIGHT BLINDNESS, CONGENITAL STATIONARY, AUTOSOMAL DOMINANT 1; CSNBAD1 PubMed Gal A, Orth U, Baehr W, ...
  2. ... no history of the disorder in their family. Autosomal dominant mental retardation 35 Genetic Testing Registry: Congenital stationary night blindness 1G National Organization for Rare Disorders (NORD) ClinicalTrials.gov HOUGE-JANSSENS SYNDROME 1; HJS1 PubMed Houge G, Haesen D, Vissers LE, ...
  3. ... the rod cGMP phosphodiesterase beta-subunit gene in autosomal dominant stationary ... to congenital stationary night blindness impairs the enzyme inhibition by ...
  4. ... stationary) over time. Unlike retinitis pigmentosa (described below), autosomal dominant congenital stationary night blindness does not affect daytime vision.The RHO gene ...
  5. ... the GNAT1 gene have been found to cause autosomal dominant congenital stationary night blindness, which is characterized by the inability to see ... active mutant of rod alpha-transducin (GNAT1) in autosomal dominant congenital stationary night blindness. Hum Mutat. 2007 Jul;28(7):741-2. ...
  6. ... include nearsightedness as a feature. These conditions include autosomal recessive congenital stationary night blindness, X-linked congenital stationary night blindness, Stickler syndrome, ...