(Q50336767)

English

Mutations in RGR, encoding a light-sensitive opsin homologue, in patients with retinitis pigmentosa.

scientific article published in December 1999

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

5 March 2018

http://europepmc.org/abstract/MED/10581022

Mutations in RGR, encoding a light-sensitive opsin homologue, in patients with retinitis pigmentosa. (English)

1 reference

Europe PubMed Central

PubMed publication ID

5 March 2018

http://europepmc.org/abstract/MED/10581022

author name string

Morimura H

1

1 reference

Europe PubMed Central

PubMed publication ID

5 March 2018

http://europepmc.org/abstract/MED/10581022

Saindelle-Ribeaudeau F

2

1 reference

Europe PubMed Central

PubMed publication ID

5 March 2018

http://europepmc.org/abstract/MED/10581022

Berson EL

3

1 reference

Europe PubMed Central

PubMed publication ID

5 March 2018

http://europepmc.org/abstract/MED/10581022

Dryja TP

4

1 reference

Europe PubMed Central

PubMed publication ID

5 March 2018

http://europepmc.org/abstract/MED/10581022

language of work or name

0 references

publication date

1 December 1999

1 reference

Europe PubMed Central

PubMed publication ID

5 March 2018

http://europepmc.org/abstract/MED/10581022

Nature Genetics

1 reference

Europe PubMed Central

PubMed publication ID

5 March 2018

http://europepmc.org/abstract/MED/10581022

23

1 reference

Europe PubMed Central

PubMed publication ID

5 March 2018

http://europepmc.org/abstract/MED/10581022

4

1 reference

Europe PubMed Central

PubMed publication ID

5 March 2018

http://europepmc.org/abstract/MED/10581022

393-394

1 reference

Europe PubMed Central

PubMed publication ID

5 March 2018

http://europepmc.org/abstract/MED/10581022

https://scigraph.springernature.com/pub.10.1038/70496

0 references

A human opsin-related gene that encodes a retinaldehyde-binding protein

1 reference

https://api.crossref.org/works/10.1038%2F70496

7 January 2021

based on heuristic

inferred from DOI database lookup

Cytoplasmic retinal localization of an evolutionary homolog of the visual pigments

1 reference

https://api.crossref.org/works/10.1038%2F70496

7 January 2021

based on heuristic

inferred from DOI database lookup

Blue and ultraviolet light-absorbing opsin from the retinal pigment epithelium

1 reference

https://api.crossref.org/works/10.1038%2F70496

7 January 2021

based on heuristic

inferred from DOI database lookup

The endogenous chromophore of retinal G protein-coupled receptor opsin from the pigment epithelium

1 reference

https://api.crossref.org/works/10.1038%2F70496

7 January 2021

based on heuristic

inferred from DOI database lookup

Localization of the humanRGR opsin gene to chromosome 10q23

1 reference

https://api.crossref.org/works/10.1038%2F70496

7 January 2021

based on heuristic

inferred from DOI database lookup

Rhodopsin mutations in autosomal dominant retinitis pigmentosa

1 reference

https://api.crossref.org/works/10.1038%2F70496

7 January 2021

based on heuristic

inferred from DOI database lookup

Disease sequence from mutant rhodopsin allele to rod and cone photoreceptor degeneration in man.

1 reference

https://api.crossref.org/works/10.1038%2F70496

7 January 2021

based on heuristic

inferred from DOI database lookup

Functional heterogeneity of mutant rhodopsins responsible for autosomal dominant retinitis pigmentosa

1 reference

https://api.crossref.org/works/10.1038%2F70496

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

1 reference

Europe PubMed Central

PubMed publication ID

5 March 2018

http://europepmc.org/abstract/MED/10581022

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

5 March 2018

http://europepmc.org/abstract/MED/10581022

ResearchGate publication ID

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