Discover Community Create You

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

Mutations in known genes account for 58% of autosomal dominant retinitis pigmentosa (adRP).

Advances in experimental medicine and biology - 1 Jan 2008

Daiger Stephen P, Sullivan Lori S, Gire Anisa I, Birch David G, Heckenlively John R, Bowne Sara J

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Gene Deletion
Share to Gene Dosage
Share to Genes, Dominant
Share to Genes, X-Linked

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Genetic Diseases, X-Linked

Share to Genetic Linkage

Share to Genetic Testing

Share to Retinitis Pigmentosa

Source

Open in PubMed Open full text

Identifiers

PMID: 18188946
DOI: 10.1007/978-0-387-74904-4_23
PMCID: PMC2582019

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 23 Oct 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Mutations in known genes account for 58% of autosomal dominant retinitis pigmentosa (adRP).PMID 18188946Read ↗

Genes and Mutations Causing Autosomal Dominant Retinitis Pigmentosa.Semantic proximity Read ↗

Autosomal Dominant Retinitis Pigmentosa.Semantic proximity Read ↗

Retinitis Pigmentosa: Genes and Disease MechanismsSemantic proximity Read ↗

Prevalence of mutations in eyeGENE probands with a diagnosis of autosomal dominant retinitis pigmentosa.Semantic proximity Read ↗

Retinitis pigmentosa and allied conditions today: a paradigm of translational researchSemantic proximity Read ↗

History of Finding Genes and Mutations Causing Inherited Retinal Diseases.Semantic proximity Read ↗

Genes Associated with Retinitis Pigmentosa and Allied Diseases Are Frequently Mutated in the General PopulationSemantic proximity Read ↗

Genes and mutations causing retinitis pigmentosa.Semantic proximity Read ↗

Non-syndromic inherited retinal diseases in Poland: Genes, mutations, and phenotypes.Semantic proximity Read ↗

Comparison of Worldwide Disease Prevalence and Genetic Prevalence of Inherited Retinal Diseases and Variant Interpretation Considerations.Semantic proximity Read ↗

Molecular genetics of retinitis pigmentosaSemantic proximity Read ↗

Gene mutations in retinitis pigmentosa and their clinical implications.Semantic proximity Read ↗

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