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Article

Enamel Anomalies in a Pachyonychia Congenita Patient with a Mutation in KRT16.

The Journal of investigative dermatology - 1 Jan 2019

Duverger Olivier, Cross Michael A, Smith Frances J D, Morasso Maria I

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Topics

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

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Identifiers

PMID: 30009827
DOI: 10.1016/j.jid.2018.07.005
PMCID: PMC11058062

Genes

KRT16

Provenance

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

Related research

Semantic proximity does not establish scientific evidence.

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Enamel Anomalies in a Pachyonychia Congenita Patient with a Mutation in KRT16.PMID 30009827Read ↗

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

Genetic variants in pachyonychia congenita-associated keratins increase susceptibility to tooth decay.Semantic proximity Read ↗

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

Insights into genotype-phenotype correlation in pachyonychia congenita from the human intermediate filament mutation database.Semantic proximity Read ↗

The genetic basis of pachyonychia congenita.Semantic proximity Read ↗

A new type of pachyonychia congenita.Semantic proximity Read ↗

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

Clinical and pathological features of pachyonychia congenita.Semantic proximity Read ↗

Recurrent mutation in keratin 17 in a large family with 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 ↗

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

Teeth anomalies and genetics, including genetic syndromesSemantic proximity Read ↗

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