Mutations in the human retinal degeneration slow (RDS) gene can cause either retinitis pigmentosa or macular dystrophy (Q28268707)

1

0 references

J Wroblewski

2

0 references

J Keen

3

0 references

C Inglehearn

4

0 references

C Jubb

5

0 references

A Eckstein

6

0 references

M Jay

7

0 references

S Bhattacharya

9

0 references

F Fitzke

A three-base-pair deletion in the peripherin–RDS gene in one form of retinitis pigmentosa

10

0 references

language of work or name

English

0 references

publication date

March 1993

0 references

published in

Nature Genetics

0 references

volume

3

0 references

issue

3

0 references

page(s)

213-8

0 references

cites work

1 reference

https://api.crossref.org/works/10.1038/NG0393-213

Mutations in the human retinal degeneration slow gene in autosomal dominant retinitis pigmentosa

21 April 2017

1 reference

https://api.crossref.org/works/10.1038/NG0393-213

Identification of a photoreceptor-specific mRNA encoded by the gene responsible for retinal degeneration slow (rds)

21 April 2017

1 reference

https://api.crossref.org/works/10.1038/NG0393-213

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

21 April 2017

1 reference

https://api.crossref.org/works/10.1038%2FNG0393-213

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0393-213

The retinal degeneration slow (rds) gene product is a photoreceptor disc membrane-associated glycoprotein.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0393-213

Localization of peripherin/rds in the disk membranes of cone and rod photoreceptors: relationship to disk membrane morphogenesis and retinal degeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0393-213

Electroretinograms evoked in man by local uniform or patterned stimulation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0393-213

Automated Light- and Dark- Adapted Perimetry for Evaluating Retinitis Pigmentosa

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0393-213

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0393-213

7 January 2021

Rhodopsin mutations in autosomal dominant retinitis pigmentosa

1 reference

https://api.crossref.org/works/10.1038%2FNG0393-213

7 January 2021

Autosomal dominant retinitis pigmentosa: Four new mutations in rhodopsin, one of them in the retinal attachment site

1 reference

https://api.crossref.org/works/10.1038%2FNG0393-213

7 January 2021

A completed screen for mutations of the rhodopsin gene in a panel of patients with autosomal dominant retinitis pigmentosa

1 reference

https://api.crossref.org/works/10.1038%2FNG0393-213

7 January 2021

Linkage mapping of autosomal dominant retinitis pigmentosa (RP1) to the pericentric region of human chromosome 8.

1 reference

https://api.crossref.org/works/10.1038%2FNG0393-213

7 January 2021

Autosomal dominant retinitis pigmentosa: a mutation in codon 178 of the rhodopsin gene in two families of Celtic origin

1 reference

https://api.crossref.org/works/10.1038%2FNG0393-213

7 January 2021

Rapid detection of single base mismatches as heteroduplexes on Hydrolink gels

1 reference

https://api.crossref.org/works/10.1038%2FNG0393-213

7 January 2021

Photoreceptor peripherin is the normal product of the gene responsible for retinal degeneration in the rds mouse

1 reference

https://api.crossref.org/works/10.1038%2FNG0393-213

7 January 2021

Molecular cloning, primary structure, and orientation of the vertebrate photoreceptor cell protein peripherin in the rod outer segment disk membrane

1 reference

https://api.crossref.org/works/10.1038%2FNG0393-213

7 January 2021

Cloning of the CDNA for a novel photoreceptor membrane protein (rom-1) identifies a disk rim protein family implicated in human retinopathies

1 reference

https://api.crossref.org/works/10.1038%2FNG0393-213

7 January 2021

Development and degeneration of retina in rds mutant mice: photoreceptor abnormalities in the heterozygotes

1 reference

https://api.crossref.org/works/10.1038%2FNG0393-213

7 January 2021

Development and degeneration of retina in rds mutant mice: altered disc shedding pattern in the albino heterozygotes and its relation to light exposure

1 reference

https://api.crossref.org/works/10.1038%2FNG0393-213

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0393-213

7 January 2021

Standard for clinical electroretinography. International Standardization Committee

1 reference

https://api.crossref.org/works/10.1038%2FNG0393-213

7 January 2021

A modified ERG technique and the results obtained in X-linked retinitis pigmentosa

1 reference

https://api.crossref.org/works/10.1038%2FNG0393-213

7 January 2021

Identifiers

DOI

10.1038/NG0393-213

1 reference

Consolidated OpenCitations Corpus – April 2017

1 reference

Consolidated OpenCitations Corpus – April 2017

PubMed publication ID

8485576

1 reference

Consolidated OpenCitations Corpus – April 2017