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

Progressive symmetrical erythrokeratoderma: report of two Chinese families and evaluation for mutations in the loricrin, connexin 30.3 and connexin 31 genes.

Clinical and experimental dermatology - 1 Dec 2013

Guo B-R, Sun L-D, Cui Y, Yang S, Zhang X-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 Adolescent
Share to Asian People
Share to China
Share to Connexins

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

Share to Erythema

Share to Keratosis

Share to Membrane Proteins

Share to Mutation

Source

Identifiers

PMID: 23678955
DOI: 10.1111/ced.12135

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

Progressive symmetrical erythrokeratoderma: report of two Chinese families and evaluation for mutations in the loricrin, connexin 30.3 and connexin 31 genes.PMID 23678955Read ↗

Progressive symmetrical erythrokeratoderma: report of a Turkish family and evaluation for loricrin and connexin gene mutations.Semantic proximity Read ↗

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

Erythrokeratodermia variabilis et progressiva allelic to oculo-dento-digital dysplasia.Semantic proximity Read ↗

No exonic mutations at GJB2, GJB3, GJB4, GJB6, ARS (Component B), and LOR genes responsible for a Chinese patient affected by progressive symmetric erythrokeratodermia with pseudoainhum.Semantic proximity Read ↗

Novel mutation of connexin 31 causing erythrokeratoderma variabilis.Semantic proximity Read ↗

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

Possible involvement of exon 31 alternative splicing in phenotype and severity of epidermolysis bullosa caused by mutations in PLEC1.Semantic proximity Read ↗

Recessive progressive symmetric erythrokeratoderma results from a homozygous loss-of-function mutation of KRT83 and is allelic with dominant monilethrix.Semantic proximity Read ↗

The spectrum of mutations in erythrokeratodermias--novel and de novo mutations in GJB3.Semantic proximity Read ↗

Progressive symmetric erythrokeratodermia with spinocerebellar ataxia due to ELOVL4 mutation in a Chinese family.Semantic proximity Read ↗

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

Erythrokeratodermia variabilis et progressiva.Semantic proximity Read ↗

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