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

Early severe pachyonychia congenita subtype PC-K6a with a novel mutation in the KRT6A gene.

Journal of the European Academy of Dermatology and Venereology : JEADV - 1 Feb 2017

Cammarata-Scalisi F, Natsuga K, Toyonaga E, Nishie W, Shimizu H, Avendaño A, Araque D, Da Silva G, Bellacchio E, Callea M

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 Child
Share to Keratin-6
Share to Mutation
Share to Pedigree

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 27445120
DOI: 10.1111/jdv.13800

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Early severe pachyonychia congenita subtype PC-K6a with a novel mutation in the KRT6A gene.PMID 27445120Read ↗

A novel mutation in K6b in pachyonychia congenita type 2.Semantic proximity Read ↗

A novel KRT6A mutation in a case of pachyonychia congenita from India.Semantic proximity Read ↗

Novel and recurrent keratin 6A (KRT6A) mutations in Chinese patients with pachyonychia congenita type 1.Semantic proximity Read ↗

Pachyonychia congenita in Japan: report of familial cases with a recurrent KRT16 mutation.Semantic proximity Read ↗

Mutations of KRT6A are more frequent than those of KRT16 in pachyonychia congenita type 1: report of a novel and a recently reported mutation in two unrelated Chinese families.Semantic proximity Read ↗

Focal PPK secondary to a novel KRT6C mutation (Pachyonychia congenita-K6c).Semantic proximity Read ↗

A recurrent missense mutation in the KRT16 gene causing pachyonychia congenita in a patient.Semantic proximity Read ↗

[Pachyonychia congenita. Molecular genetic analysis simplifies clinical classification in subtypes].Semantic proximity Read ↗

[Pachyonychia congenita type 2 due to mutation in the keratin 6b gene].Semantic proximity Read ↗

Mutation of a type II keratin gene (K6a) in pachyonychia congenitaSemantic proximity Read ↗

Revisiting pachyonychia congenita: a case-cohort study of 815 patients.Semantic proximity Read ↗

KRT6A Variant Underlies Pachyonychia Congenita: Insights Into Protein Aggregation and PPAR Signaling.Semantic proximity Read ↗

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