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 and recurrent mutations in the 1B domain of keratin 1 in palmoplantar keratoderma with tonotubules.

The British journal of dermatology - 1 Feb 2009

Grimberg G, Hausser I, Müller F B, Wodecki K, Schaffrath C, Krieg T, Oji V, Traupe H, Arin M 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 Child, Preschool
Share to Keratoderma, Palmoplantar
Share to Mutation
Share to Pain

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Pedigree

Share to Recurrence

Source

Identifiers

PMID: 18795921
DOI: 10.1111/j.1365-2133.2008.08831.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 and recurrent mutations in the 1B domain of keratin 1 in palmoplantar keratoderma with tonotubules.PMID 18795921Read ↗

Expanding the keratin mutation database: novel and recurrent mutations and genotype-phenotype correlations in 28 patients with epidermolytic ichthyosis.Semantic proximity Read ↗

Mutations in the highly conserved 1A rod domain of keratin 9 responsible for epidermolytic palmoplantar keratoderma in four Chinese families.Semantic proximity Read ↗

Human keratin diseases: the increasing spectrum of disease and subtlety of the phenotype-genotype correlation.Semantic proximity Read ↗

Two cases of primarily palmoplantar keratoderma associated with novel mutations in keratin 1.Semantic proximity Read ↗

Novel splice site mutation in keratin 1 underlies mild epidermolytic palmoplantar keratoderma in three kindreds.Semantic proximity Read ↗

A novel mutation of the keratin 1 gene in a family with epidermolytic hyperkeratosis.Semantic proximity Read ↗

Mutation L437P in the 2B domain of keratin 1 causes diffuse palmoplantar keratoderma in a Chinese pedigree.Semantic proximity Read ↗

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

Striate palmoplantar keratoderma: Report of a novel DSG1 mutation and atypical clinical manifestations.Semantic proximity Read ↗

Epidermolytic palmoplantar keratoderma of Vörner: re-evaluation of Vörner's original family and identification of a novel keratin 9 mutationSemantic proximity Read ↗

New and recurrent AAGAB mutations in punctate palmoplantar keratoderma.Semantic proximity Read ↗

Identification of a novel causative mutation in KRT1 in diffuse palmoplantar keratoderma, facilitated by whole-exome sequencing.Semantic proximity Read ↗

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