Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Incidence of the gene mutation causal for rod-cone dysplasia type 1 in Irish setters in the UK.

The Journal of small animal practice - 1 Jul 1995

Petersen-Jones S M, Clements P J, Barnett K C, Sargan D R

Abstract excerpt

A survey to establish the UK prevalence of the gene mutation causing the rod-cone dysplasia type one (rcd1) form of generalised progressive retinal atrophy (gPRA) in Irish setters was carried out. The dogs were selected by members of two Irish setter breed societies to provide examples from most of the main breeding lines in the UK. A total of 210 Irish setters were tested and one bitch was found to be a carrier...

Topics

Animals
Base Sequence
DNA Primers
DNA Restriction Enzymes
Dog Diseases
Dogs
Female
Male
Molecular Sequence Data
Mutation
Polymerase Chain Reaction
Retinal Dysplasia

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

United Kingdom

Source

Identifiers

PMID: 7474961
DOI: 10.1111/j.1748-5827.1995.tb02934.x

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 29 Aug 2026. Prepared record publication-7474961-2026-08-29.1. Manifest publication-graph-cohort-2026-08-29.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 29 Aug 2026.

Community interpretation

Discuss the evidence

Ask a question, add context or challenge an interpretation. Community activity is separate from scientific evidence strength.

0

discussions

0

replies

Citations encouraged

Claims remain attributable.

No discussion yet

Be the first to add a careful, cited interpretation.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Incidence of the gene mutation causal for rod-cone dysplasia type 1 in Irish setters in the UK.PMID 7474961Read ↗

Familial non-rcd1 generalised retinal degeneration in Irish setters.Semantic proximity Read ↗

Late-onset progressive retinal atrophy in the Gordon and Irish Setter breeds is associated with a frameshift mutation in C2orf71.Semantic proximity Read ↗

Molecular diagnostic tests for ascertainment of genotype at the rod cone dysplasia 1 (rcd1) locus in Irish setters.Semantic proximity Read ↗

Frequency of the codon 807 mutation in the cGMP phosphodiesterase beta-subunit gene in Irish setters and other dog breeds with hereditary retinal degeneration.Semantic proximity Read ↗

Genetic screening for progressive retinal atrophy in the Australian population of Irish Setters.Semantic proximity Read ↗

The incidence of genetic disease alleles in Australian Shepherd dog breed in European countries.Semantic proximity Read ↗

Cosegregation of codon 807 mutation of the canine rod cGMP phosphodiesterase beta gene and rcd1.Semantic proximity Read ↗

Irish setter dogs affected with rod/cone dysplasia contain a nonsense mutation in the rod cGMP phosphodiesterase beta-subunit gene.Semantic proximity Read ↗

A review of research to elucidate the causes of the generalized progressive retinal atrophies.Semantic proximity Read ↗

Ophthalmic and cone derived electrodiagnostic findings in outbred Miniature Long-haired Dachshunds homozygous for a RPGRIP1 mutation.Semantic proximity Read ↗

An epidemiological approach to prevention and control of three common heritable diseases in canine pedigree breeds in the United Kingdom.Semantic proximity Read ↗

Genetic screening for PRA-associated mutations in multiple dog breeds shows that PRA is heterogeneous within and between breeds.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.