(Q48069393)

8 February 2018

title

Canine homolog and exclusion of retinal degeneration slow (rds) as the gene for early retinal degeneration (erd) in the dog. (English)

1 reference

8 February 2018

1 reference

Moghrabi WN

1

1 reference

8 February 2018

Kedzierski W

series ordinal

2

1 reference

8 February 2018

Travis GH

series ordinal

3

1 reference

8 February 2018

publication date

1 November 1995

1 reference

8 February 2018

Experimental Eye Research

published in

1 reference

8 February 2018

volume

61

1 reference

8 February 2018

issue

5

1 reference

8 February 2018

page(s)

641-643

1 reference

8 February 2018

Non-allelism of three genes (rcd1, rcd2 and erd) for early-onset hereditary retinal degeneration

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0014-4835%2805%2980059-4

Retinal degenerations in the dog: IV. Early retinal degeneration (erd) in Norwegian elkhounds

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-4835%2805%2980059-4

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-4835%2805%2980059-4

Nucleotide and predicted protein sequence of rat retinal degeneration slow (rds).

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-4835%2805%2980059-4

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-4835%2805%2980059-4

The cat RDS transcript: candidate gene analysis and phylogenetic sequence analysis.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-4835%2805%2980059-4

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-4835%2805%2980059-4

A null mutation in the human peripherin/RDS gene in a family with autosomal dominant retinitis punctata albescens

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-4835%2805%2980059-4

Retinal pattern dystrophy associated with a 4 bp insertion at codon 140 in the RDS-peripherin gene

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-4835%2805%2980059-4

Butterfly-shaped pigment dystrophy of the fovea caused by a point mutation in codon 167 of the RDS gene

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-4835%2805%2980059-4

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-4835%2805%2980059-4

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-4835%2805%2980059-4

The human retinal degeneration slow (RDS) gene: Chromosome assignment and structure of the mRNA

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-4835%2805%2980059-4

A new H-2-linked mutation, rds, causing retinal degeneration in the mouse

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-4835%2805%2980059-4

Phenotypic Variation Including Retinitis Pigmentosa, Pattern Dystrophy, and Fundus Flavimaculatus in a Single Family With a Deletion of Codon 153 or 154 of the Peripherin/RDS Gene

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-4835%2805%2980059-4

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-4835%2805%2980059-4

Macular dystrophy associated with mutations at codon 172 in the human retinal degeneration slow gene

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-4835%2805%2980059-4

10.1016/S0014-4835(05)80059-4

7 January 2021

Identifiers

DOI

1 reference

8 February 2018

PubMed ID

8654508

1 reference

8 February 2018