Total colourblindness is caused by mutations in the gene encoding the alpha-subunit of the cone photoreceptor cGMP-gated cation channel (Q28115254)

1

0 references

author name string

T. Marx

2

1 reference

3 January 2017

H. Jägle

4

1 reference

3 January 2017

S. G. Jacobson

5

1 reference

3 January 2017

E. Apfelstedt-Sylla

6

1 reference

3 January 2017

E. Zrenner

7

1 reference

3 January 2017

L. T. Sharpe

8

1 reference

3 January 2017

B. Wissinger

Homozygosity mapping of achromatopsia to chromosome 2 using DNA pooling

9

1 reference

3 January 2017

language of work or name

English

0 references

publication date

1 July 1998

1 reference

3 January 2017

1 reference

3 January 2017

19

1 reference

3 January 2017

257–259

1 reference

3 January 2017

3

1 reference

3 January 2017

1 reference

7 January 2021

Molecular cloning, functional expression and chromosomal localization of a human homolog of the cyclic nucleotide-gated ion channel of retinal cone photoreceptors

1 reference

7 January 2021

Cloning, chromosomal localization and functional expression of the gene encoding the alpha-subunit of the cGMP-gated channel in human cone photoreceptors

1 reference

7 January 2021

Human rod monochromacy: linkage analysis and mapping of a cone photoreceptor expressed candidate gene on chromosome 2q11

1 reference

7 January 2021

A putative cyclic nucleotide-gated channel is required for sensory development and function in C. elegans

1 reference

7 January 2021

Cloning and functional expression of a cyclic-nucleotide-gated channel from mammalian sperm

1 reference

7 January 2021

Rod and cone photoreceptor cells express distinct genes for cGMP-gated channels.

1 reference

7 January 2021

Structure and function of cyclic nucleotide-gated channels

1 reference

7 January 2021

Cyclic GMP contact points within the 63-kDa subunit and a 240-kDa associated protein of retinal rod cGMP-activated channels

1 reference

7 January 2021

Mutations in the gene encoding the alpha subunit of the rod cGMP-gated channel in autosomal recessive retinitis pigmentosa

1 reference

7 January 2021

Heterozygous missense mutation in the rhodopsin gene as a cause of congenital stationary night blindness

1 reference

7 January 2021

Photoreceptor degeneration in vitamin A deprivation and retinitis pigmentosa: the equivalent light hypothesis.

1 reference

7 January 2021

A mutation in guanylate cyclase activator 1A (GUCA1A) in an autosomal dominant cone dystrophy pedigree mapping to a new locus on chromosome 6p21.1

1 reference

7 January 2021

A null mutation in the photoreceptor guanylate cyclase gene causes the retinal degeneration chicken phenotype

1 reference

7 January 2021