(Q28116005)

4 January 2017

title

Defective colour vision associated with a missense mutation in the human green visual pigment gene (English)

1 reference

4 January 2017

J. Winderickx

1

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4 January 2017

E. Sanocki

2

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4 January 2017

D. T. Lindsey

3

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4 January 2017

D. Y. Teller

4

1 reference

4 January 2017

A. G. Motulsky

5

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4 January 2017

S. S. Deeb

6

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4 January 2017

language of work or name

English

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publication date

1 July 1992

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4 January 2017

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4 January 2017

volume

1

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4 January 2017

issue

4

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4 January 2017

page(s)

251–256

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Molecular biology of the visual pigments

4 January 2017

cites work

1 reference

https://api.crossref.org/works/10.1038/NG0792-251

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

21 April 2017

1 reference

https://api.crossref.org/works/10.1038%2FNG0792-251

A point mutation of the rhodopsin gene in one form of retinitis pigmentosa

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0792-251

Polymorphism in red photopigment underlies variation in colour matching

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0792-251

Molecular patterns of X chromosome-linked color vision genes among 134 men of European ancestry

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0792-251

7 January 2021

Old and new genetics help ordering loci at the telomere of the human X-chromosome long arm

1 reference

https://api.crossref.org/works/10.1038%2FNG0792-251

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%2FNG0792-251

7 January 2021

Tandem array of human visual pigment genes at Xq28

1 reference

https://api.crossref.org/works/10.1038%2FNG0792-251

7 January 2021

A 195-kb cosmid walk encompassing the human Xq28 color vision pigment genes

1 reference

https://api.crossref.org/works/10.1038%2FNG0792-251

7 January 2021

Molecular genetics of inherited variation in human color vision

1 reference

https://api.crossref.org/works/10.1038%2FNG0792-251

7 January 2021

Cysteine residues 110 and 187 are essential for the formation of correct structure in bovine rhodopsin

1 reference

https://api.crossref.org/works/10.1038%2FNG0792-251

7 January 2021

Model systems for the study of seven-transmembrane-segment receptors

1 reference

https://api.crossref.org/works/10.1038%2FNG0792-251

7 January 2021

The structure of bovine rhodopsin

1 reference

https://api.crossref.org/works/10.1038%2FNG0792-251

7 January 2021

Molecular genetics of human blue cone monochromacy

1 reference

https://api.crossref.org/works/10.1038%2FNG0792-251

7 January 2021

Molecular genetics of X chromosome-linked color vision among populations of African and Japanese ancestry: high frequency of a shortened red pigment gene among Afro-Americans

1 reference

https://api.crossref.org/works/10.1038%2FNG0792-251

7 January 2021

Rhodopsin mutations in autosomal dominant retinitis pigmentosa

1 reference

https://api.crossref.org/works/10.1038%2FNG0792-251

7 January 2021

Mutation spectrum of the rhodopsin gene among patients with autosomal dominant retinitis pigmentosa

1 reference

https://api.crossref.org/works/10.1038%2FNG0792-251

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0792-251

7 January 2021

Two different genes for X-linked retinitis pigmentosa

1 reference

https://api.crossref.org/works/10.1038%2FNG0792-251

7 January 2021

Linkage relationships between retinoschisis, Xg, and a cloned DNA sequence from the distal short arm of the X chromosome

1 reference

https://api.crossref.org/works/10.1038%2FNG0792-251

7 January 2021

X-linked retinoschisis is closely linked to DXS41 and DXS16 but not DXS85

1 reference

https://api.crossref.org/works/10.1038%2FNG0792-251

7 January 2021

Choroideremia: further evidence for assignment of the locus to Xq13-Xq21

1 reference

https://api.crossref.org/works/10.1038%2FNG0792-251

7 January 2021

Choroideremia: close linkage to DXYS1 and DXYS12 demonstrated by segregation analysis and historical-genealogical evidence

1 reference

https://api.crossref.org/works/10.1038%2FNG0792-251

7 January 2021

Detection of polymorphisms of human DNA by gel electrophoresis as single-strand conformation polymorphisms

1 reference

https://api.crossref.org/works/10.1038%2FNG0792-251

7 January 2021

DNA sequencing with chain-terminating inhibitors

1 reference

https://api.crossref.org/works/10.1038%2FNG0792-251

7 January 2021

Identifiers

DOI

10.1038/NG0792-251

0 references

1 reference