Total colourblindness is caused by mutations in the gene encoding the α-subunit of the cone photoreceptor cGMP-gated cation channel
- 1 July 1998
- journal article
- letter
- Published by Springer Science and Business Media LLC in Nature Genetics
- Vol. 19 (3), 257-259
- https://doi.org/10.1038/935
Abstract
No abstract availableThis publication has 15 references indexed in Scilit:
- Human Rod Monochromacy: Linkage Analysis and Mapping of a Cone Photoreceptor Expressed Candidate Gene on Chromosome 2q11Genomics, 1998
- Cloning, chromosomal localization and functional expression of the gene encoding the α-subunit of the cGMP-gated channel in human cone photoreceptorsEuropean Journal of Neuroscience, 1997
- Homozygosity Mapping of Achromatopsia to Chromosome 2 Using DNA PoolingHuman Molecular Genetics, 1997
- A Putative Cyclic Nucleotide–Gated Channel Is Required for Sensory Development and Function in C. elegansNeuron, 1996
- Molecular cloning, functional expression and chromosomal localization of a human homolog of the cyclic nucleotide‐gated ion channel of retinal cone photoreceptorsFEBS Letters, 1996
- Structure and Function of Cyclic Nucleotide-Gated ChannelsAnnual Review of Neuroscience, 1996
- Cyclic GMP contact points within the 63-kDa subunit and a 240-kDa associated protein of retinal rod cGMP-activated channelsBiochemistry, 1995
- Cloning and functional expression of a cyclic-nucleotide-gated channel from mammalian spermNature, 1994
- Rod and cone photoreceptor cells express distinct genes for cGMP-gated channelsNeuron, 1993
- Primary structure and chromosomal localization of human and mouse rod photoreceptor cGMP-gated cation channel.Online Journal of Public Health Informatics, 1992