Loss of the Effector Function in a Transducin-α Mutant Associated with Nougaret Night Blindness
Open Access
- 1 March 2000
- journal article
- Published by Elsevier in Journal of Biological Chemistry
- Vol. 275 (10), 6969-6974
- https://doi.org/10.1074/jbc.275.10.6969
Abstract
No abstract availableKeywords
This publication has 45 references indexed in Scilit:
- Missense mutation in the gene encoding the α subunit of rod transducin in the Nougaret form of congenital stationary night blindnessNature Genetics, 1996
- How photons start vision.Proceedings of the National Academy of Sciences, 1996
- Autosomal recessive retinitis pigmentosa caused by mutations in the α subunit of rod cGMP phosphodiesteraseNature Genetics, 1995
- Mutations in the gene encoding the alpha subunit of the rod cGMP-gated channel in autosomal recessive retinitis pigmentosa.Proceedings of the National Academy of Sciences, 1995
- Mutation spectrum of the gene encoding the beta subunit of rod phosphodiesterase among patients with autosomal recessive retinitis pigmentosa.Proceedings of the National Academy of Sciences, 1995
- 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 rod cGMP phosphodiesterase β–subunit gene in autosomal dominant stationary night blindnessNature Genetics, 1994
- Heterozygous missense mutation in the rhodopsin gene as a cause of congenital stationary night blindnessNature Genetics, 1993
- Mutation spectrum of the rhodopsin gene among patients with autosomal dominant retinitis pigmentosa.Proceedings of the National Academy of Sciences, 1991
- Molecular mechanism of visual transductionEuropean Journal of Biochemistry, 1989