Colour vision deficiency (Q35013819)

5 August 2017

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title

Colour vision deficiency (English)

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5 August 2017

M P Simunovic

1

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5 August 2017

20 November 2009

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5 August 2017

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5 August 2017

24

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5 August 2017

5

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5 August 2017

747-755

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https://scigraph.springernature.com/pub.10.1038/eye.2009.251

5 August 2017

0 references

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2009.251

Analysis of L-cone/M-cone visual pigment gene arrays in Japanese males with protan color-vision deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2009.251

A novel mutation in the short-wavelength-sensitive cone pigment gene associated with a tritan color vision defect

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2009.251

Congenital X-linked incomplete achromatopsia. Evidence for slow progression, carrier fundus findings, and possible genetic linkage with glucose-6-phosphate dehydrogenase locus

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2009.251

The X-Chrom lens. On seeing red.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2009.251

Human visual pigments: microspectrophotometric results from the eyes of seven persons

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2009.251

7 January 2021

The machinery of colour vision

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2009.251

7 January 2021

Color vision: opsins and options

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2009.251

7 January 2021

The koniocellular pathway in primate vision

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2009.251

7 January 2021

Multidimensional scaling reveals a color dimension unique to 'color-deficient' observers.

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2009.251

7 January 2021

Functional photoreceptor loss revealed with adaptive optics: an alternate cause of color blindness

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2009.251

7 January 2021

Adaptive optics retinal imaging reveals S-cone dystrophy in tritan color-vision deficiency

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2009.251

7 January 2021

X-linked cone dysfunction syndrome with myopia and protanopia

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2009.251

7 January 2021

https://api.crossref.org/works/10.1038%2FEYE.2009.251

1 reference

7 January 2021

Classification of complete and incomplete autosomal recessive achromatopsia

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2009.251

7 January 2021

Thermal vasomotor responses in human skin mediated by local mechanisms

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2009.251

7 January 2021

The electroretinogram of a cone-monochromat

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2009.251

7 January 2021

https://api.crossref.org/works/10.1038%2FEYE.2009.251

1 reference

7 January 2021

Molecular genetics of human color vision: the genes encoding blue, green, and red pigments

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2009.251

7 January 2021

Molecular genetics of inherited variation in human color vision

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2009.251

7 January 2021

The molecular basis of dichromatic color vision in males with multiple red and green visual pigment genes

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2009.251

7 January 2021

Novel missense mutations in red/green opsin genes in congenital color-vision deficiencies.

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2009.251

7 January 2021

An A-71C substitution in a green gene at the second position in the red/green visual-pigment gene array is associated with deutan color-vision deficiency

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2009.251

7 January 2021

An electroretinographic and molecular genetic study of X-linked cone degeneration

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2009.251

7 January 2021

Spectral tuning of pigments underlying red-green color vision

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2009.251

7 January 2021

Role of hydroxyl-bearing amino acids in differentially tuning the absorption spectra of the human red and green cone pigments

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2009.251

7 January 2021

A study of women heterozygous for colour deficiencies.

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2009.251

7 January 2021

The genetics of tritan disturbances.

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2009.251

7 January 2021

The characteristics of tritanopia.

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2009.251

7 January 2021

Molecular genetics of human blue cone monochromacy

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2009.251

7 January 2021

Blue cone monochromatism: a phenotype and genotype assessment with evidence of progressive loss of cone function in older individuals

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2009.251

7 January 2021

A new mechanism in blue cone monochromatism

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2009.251

7 January 2021

Gene conversion between red and defective green opsin gene in blue cone monochromacy

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2009.251

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2009.251

7 January 2021

Mutations in the CNGB3 gene encoding the beta-subunit of the cone photoreceptor cGMP-gated channel are responsible for achromatopsia (ACHM3) linked to chromosome 8q21.

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2009.251

7 January 2021

Mutations in the cone photoreceptor G-protein alpha-subunit gene GNAT2 in patients with achromatopsia

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2009.251

7 January 2021

Disruption of conserved rhodopsin disulfide bond by Cys187Tyr mutation causes early and severe autosomal dominant retinitis pigmentosa

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2009.251

7 January 2021

The cone dysfunction syndromes

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2009.251

7 January 2021

Clinical features of achromatopsia in Swedish patients with defined genotypes

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2009.251

7 January 2021

CNGB3 achromatopsia with progressive loss of residual cone function and impaired rod-mediated function.

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2009.251

7 January 2021

Account of a Case of Defective Power to distinguish Colours.

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2009.251

7 January 2021

THE DARK ADAPTATION OF THE COLOR ANOMALOUS MEASURED WITH LIGHTS OF DIFFERENT HUES.

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2009.251

7 January 2021

Protan colour vision deficiency and road accidents

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2009.251

7 January 2021

Discrimination of binocular color mixtures in dichromacy: evaluation of the Maxwell-Cornsweet conjecture.

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2009.251

7 January 2021

The psychophysics of detecting binocular discrepancies of luminance

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2009.251

7 January 2021

Long wavelength pass filters designed for the management of color vision deficiencies

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2009.251

7 January 2021

The ChromaGen contact lens system: colour vision test results and subjective responses

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2009.251

7 January 2021

Restoration of cone vision in a mouse model of achromatopsia

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2009.251

7 January 2021

Optical coherence tomography of the macula in congenital achromatopsia

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2009.251

7 January 2021

In vivo imaging of the photoreceptor mosaic of a rod monochromat

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2009.251

7 January 2021

Reorganization of human cortical maps caused by inherited photoreceptor abnormalities.

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2009.251

7 January 2021

Gene therapy for red-green colour blindness in adult primates

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2009.251

7 January 2021

Identifiers

DOI

10.1038/EYE.2009.251

1 reference

5 August 2017

1 reference

PubMed ID

19927164