Congenital stationary night blindness associated with mutations in GRM6 encoding glutamate receptor MGluR6

This publication has 10 references indexed in Scilit:

• Night blindness and abnormal cone electroretinogram ON responses in patients with mutations in the GRM6 gene encoding mGluR6
  Proceedings of the National Academy of Sciences, 2005
• Genotype-phenotype correlation in British families with X linked congenital stationary night blindness
  British Journal of Ophthalmology, 2003
• Mutations in theCACNA1F andNYX genes in British CSNBX families
  Human Mutation, 2003
• Phenotypic expression of the complete type of X-linked congenital stationary night blindness in patients with different mutations in the NYX gene
  Albrecht von Graefes Archiv für Ophthalmologie, 2002
• A novel mutation within the rhodopsin gene (Thr-94-Ile) causing autosomal dominant congenital stationary night blindness
  Human Mutation, 1999
• Dark-light: model for nightblindness from the human rhodopsin Gly-90-->Asp mutation.
  Proceedings of the National Academy of Sciences, 1995
• Heterozygous missense mutation in the rhodopsin gene as a cause of congenital stationary night blindness
  Nature Genetics, 1993
• Molecular characterization of a novel retinal metabotropic glutamate receptor mGluR6 with a high agonist selectivity for L-2-amino-4-phosphonobutyrate
  Journal of Biological Chemistry, 1993
• Functions of the ON and OFF channels of the visual system
  Nature, 1986
• 2-Amino-4-Phosphonobutyric Acid: A New Pharmacological Tool for Retina Research
  Science, 1981