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

Novel mutation of connexin 31 causing erythrokeratoderma variabilis.

The British journal of dermatology - 1 May 2005

Feldmeyer L, Plantard L, Mevorah B, Huber M, Hohl D

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 Aged
Share to Base Sequence
Share to Connexins
Share to Keratosis

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Mutation

Share to Pedigree

Share to Skin Diseases, Genetic

Source

Identifiers

PMID: 15888179
DOI: 10.1111/j.1365-2133.2005.06561.x

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Novel mutation of connexin 31 causing erythrokeratoderma variabilis.PMID 15888179Read ↗

A case of erythrokeratodermia variabilis with connexin 31 gene mutation (Cx31F137L).Semantic proximity Read ↗

Novel mutation in GJB4 gene (connexin 30.3) in a family with erythrokeratodermia variabilis.Semantic proximity Read ↗

Erythrokeratoderma Variabilis Caused by p.Gly45Glu in Connexin 31: Importance of the First Extracellular Loop Glycine Residue for Gap Junction Function.Semantic proximity Read ↗

Novel and recurrent connexin 30.3 and connexin 31 mutations associated with erythrokeratoderma variabilis.Semantic proximity Read ↗

Clinical and genetic heterogeneity of erythrokeratoderma variabilis.Semantic proximity Read ↗

A case of erythrokeratoderma variabilis without mutations in connexin 31.Semantic proximity Read ↗

The genetic and molecular basis of a connexin-linked skin disease.Semantic proximity Read ↗

Erythrokeratodermia variabilis.Semantic proximity Read ↗

Identification of a novel mutation R42P in the gap junction protein beta-3 associated with autosomal dominant erythrokeratoderma variabilis.Semantic proximity Read ↗

Novel variants in ABCA12 cause erythrokeratodermia variabilis.Semantic proximity Read ↗

Mutations in the human connexin gene GJB3 cause erythrokeratodermia variabilis.Semantic proximity Read ↗

Genetic heterogeneity in erythrokeratodermia variabilis: novel mutations in the connexin gene GJB4 (Cx30.3) and genotype-phenotype correlations.Semantic proximity Read ↗

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