(Q72909990)

English

A leucine to arginine amino acid substitution at codon 46 of rhodopsin is responsible for a severe form of autosomal dominant retinitis pigmentosa

scientific article published on 01 January 1993

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8364589%20AND%20SRC:MED&resulttype=core&format=json

30 October 2019

A leucine to arginine amino acid substitution at codon 46 of rhodopsin is responsible for a severe form of autosomal dominant retinitis pigmentosa (English)

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8364589%20AND%20SRC:MED&resulttype=core&format=json

30 October 2019

retinitis pigmentosa

1 reference

based on heuristic

inferred from title

author name string

J A Rodriguez

1

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8364589%20AND%20SRC:MED&resulttype=core&format=json

30 October 2019

C A Herrera

2

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8364589%20AND%20SRC:MED&resulttype=core&format=json

30 October 2019

D G Birch

3

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8364589%20AND%20SRC:MED&resulttype=core&format=json

30 October 2019

S P Daiger

4

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8364589%20AND%20SRC:MED&resulttype=core&format=json

30 October 2019

publication date

1 January 1993

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8364589%20AND%20SRC:MED&resulttype=core&format=json

30 October 2019

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8364589%20AND%20SRC:MED&resulttype=core&format=json

30 October 2019

2

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8364589%20AND%20SRC:MED&resulttype=core&format=json

30 October 2019

3

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8364589%20AND%20SRC:MED&resulttype=core&format=json

30 October 2019

205-213

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8364589%20AND%20SRC:MED&resulttype=core&format=json

30 October 2019

Standardized full-field electroretinography. Normal values and their variation with age

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380020309

7 January 2021

based on heuristic

inferred from DOI database lookup

Mutations within the rhodopsin gene in patients with autosomal dominant retinitis pigmentosa

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380020309

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380020309

7 January 2021

based on heuristic

inferred from DOI database lookup

The hydrophobic moment detects periodicity in protein hydrophobicity

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380020309

7 January 2021

based on heuristic

inferred from DOI database lookup

Autosomal dominant retinitis pigmentosa: linkage to rhodopsin and evidence for genetic heterogeneity

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380020309

7 January 2021

based on heuristic

inferred from DOI database lookup

Ocular findings associated with a rhodopsin gene codon 58 transversion mutation in autosomal dominant retinitis pigmentosa.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380020309

7 January 2021

based on heuristic

inferred from DOI database lookup

Autosomal dominant sectoral retinitis pigmentosa. Two families with transversion mutation in codon 23 of rhodopsin

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380020309

7 January 2021

based on heuristic

inferred from DOI database lookup

On the molecular genetics of retinitis pigmentosa

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380020309

7 January 2021

based on heuristic

inferred from DOI database lookup

Retinal function and rhodopsin levels in autosomal dominant retinitis pigmentosa with rhodopsin mutations

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380020309

7 January 2021

based on heuristic

inferred from DOI database lookup

Abnormal rod dark adaptation in autosomal dominant retinitis pigmentosa with proline-23-histidine rhodopsin mutation

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380020309

7 January 2021

based on heuristic

inferred from DOI database lookup

At last. A standard electroretinography protocol

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380020309

7 January 2021

based on heuristic

inferred from DOI database lookup

Autosomal dominant retinitis pigmentosa (ADRP): Localization of an ADRP gene to the long arm of chromosome 3

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380020309

7 January 2021

based on heuristic

inferred from DOI database lookup

Rhodopsin: structure, function, and genetics

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380020309

7 January 2021

based on heuristic

inferred from DOI database lookup

Rapid and sensitive detection of point mutations and DNA polymorphisms using the polymerase chain reaction

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380020309

7 January 2021

based on heuristic

inferred from DOI database lookup

Rhodopsin Thr58Arg Mutation in a Family with Autosomal Dominant Retinitis Pigmentosa

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380020309

7 January 2021

based on heuristic

inferred from DOI database lookup

A null mutation in the rhodopsin gene causes rod photoreceptor dysfunction and autosomal recessive retinitis pigmentosa

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380020309

7 January 2021

based on heuristic

inferred from DOI database lookup

DNA sequencing with chain-terminating inhibitors

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380020309

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/10.1002%2FHUMU.1380020309

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/10.1002%2FHUMU.1380020309

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1002/HUMU.1380020309

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8364589%20AND%20SRC:MED&resulttype=core&format=json

30 October 2019

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8364589%20AND%20SRC:MED&resulttype=core&format=json

30 October 2019

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q72909990&oldid=1746227041"