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

Dowling-Degos disease with mutation in the exon 1 of the keratin 5 gene.

Journal of the European Academy of Dermatology and Venereology : JEADV - 1 Jan 2018

Yu W, Gan L, Wu J, Sun J, Jiang Y

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 Exons
Share to Hyperpigmentation
Share to Keratin-5
Share to Mutation

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Skin Diseases, Genetic

Source

Identifiers

PMID: 28646612
DOI: 10.1111/jdv.14426

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Dowling-Degos disease with mutation in the exon 1 of the keratin 5 gene.PMID 28646612Read ↗

Whole exome sequencing in a multi-generation family from India reveals a genetic variation c.10C>T (p.Gln4Ter) in keratin 5 gene associated with Dowling-Degos disease.Semantic proximity Read ↗

Dowling-Degos disease: case report and review of the literature.Semantic proximity Read ↗

Atypical presentation of Dowling-Degos disease with novel and recurrent mutations in POFUT1.Semantic proximity Read ↗

[Of hair and genes: The continuing story of Dowling-Degos disease].Semantic proximity Read ↗

A case report of Dowling-Degos disease caused by POFUT1 exon deletion with possible coexistent CARD14 mutation-related psoriasis.Semantic proximity Read ↗

A mutation in exon 1 of keratin 14 resulting in a Chinese family with epidermolysis bullosa simplex Dowling-Meara.Semantic proximity Read ↗

Genome-wide linkage and exome sequencing analyses identify an initiation codon mutation of KRT5 in a unique Chinese family with generalized Dowling-Degos disease.Semantic proximity Read ↗

A novel mutation in POFUT1 gene associated with Dowling-Degos disease and hidradenitis suppurativa.Semantic proximity Read ↗

Novel keratin 5 mutations in epidermolysis bullosa simplex: cases with unusual genotype-phenotype correlation.Semantic proximity Read ↗

A recurrent keratin 14 mutation in Dowling-Meara epidermolysis bullosa simplex.Semantic proximity Read ↗

A novel keratin K5 gene mutation in Dowling-Meara epidermolysis bullosa simplex.Semantic proximity Read ↗

Novel keratin 5 and 14 gene mutations in patients with epidermolysis bullosa simplex from Poland.Semantic proximity Read ↗

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