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

Recurrent mutation in keratin 17 in a large family with pachyonychia congenita type 2.

Archives of dermatological research - 1 Jun 2008

Oh Adib Carol, Jones Brad, Liao Haihui, Smith Frances J D, Solomon Rustum, Egan Conleth A, Leachman Sancy

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 Age Factors
Share to Diagnosis, Differential
Share to Keratoderma, Palmoplantar
Share to Mutation

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Nails, Malformed

Share to Pedigree

Source

Identifiers

PMID: 18347808
DOI: 10.1007/s00403-008-0840-7

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Recurrent mutation in keratin 17 in a large family with pachyonychia congenita type 2.PMID 18347808Read ↗

Identification of two recurrent mutations in keratin genes in three cases with pachyonychia congenita.Semantic proximity Read ↗

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

Pachyonychia congenita type 2: keratin 17 mutation in a Japanese case.Semantic proximity Read ↗

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

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

Novel and recurrent mutations in the genes encoding keratins K6a, K16 and K17 in 13 cases of pachyonychia congenita.Semantic proximity Read ↗

Mutation report: identification of a germline mutation in keratin 17 in a family with pachyonychia congenita type 2.Semantic proximity Read ↗

Pachyonychia congenita type 2, N92S mutation of keratin 17 gene: clinical features, mutation analysis and pathological view.Semantic proximity Read ↗

Novel keratin 17 mutations in pachyonychia congenita type 2.Semantic proximity Read ↗

The genetic basis of pachyonychia congenita.Semantic proximity Read ↗

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

[Keratin 17 mutation in pachyonychia congenita type 2 in a Chinese Han family].Semantic proximity Read ↗

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