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Article

The common KRT9 gene mutation in a Japanese patient with epidermolytic palmoplantar keratoderma and knuckle pad-like keratoses.

The Journal of dermatology - 1 Jun 2005

Hamada Takahiro, Ishii Norito, Karashima Tadashi, Kawano Yuko, Yasumoto Shinichiro, Hashimoto Takashi

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 16043929
DOI: 10.1111/j.1346-8138.2005.tb00789.x

Genes

KRT9

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

The common KRT9 gene mutation in a Japanese patient with epidermolytic palmoplantar keratoderma and knuckle pad-like keratoses.PMID 16043929Read ↗

Nonsense mutations in KRT1 caused recessive epidermolytic palmoplantar keratoderma with knuckle pads.Semantic proximity Read ↗

Novel mutation of the KRT 10 gene in a Japanese patient with epidermolytic hyperkeratosis.Semantic proximity Read ↗

An in-frame 18 bp deletion in linker domain L1 of KRT9 identified in a Japanese patient with epidermolytic palmoplantar keratoderma.Semantic proximity Read ↗

The P25L mutation in the KRT5 gene in a Japanese family with epidermolysis bullosa simplex with mottled pigmentation.Semantic proximity Read ↗

Cohen syndrome coincident with epidermolytic palmoplantar keratoderma caused by novel KRT9 gene mutation: A rare case report.Semantic proximity Read ↗

[Present status of the molecular genetics in epidermolytic 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 ↗

A novel mutation of keratin 9 in a large Chinese family with epidermolytic palmoplantar keratoderma.Semantic proximity Read ↗

Superficial epidermolytic ichthyosis caused by a novel KRT2 mutation.Semantic proximity Read ↗

Two homozygous KRT85 mutations in a Chinese patient with pure hair and nail ectodermal dysplasia.Semantic proximity Read ↗

Mild epidermolytic ichthyosis with palmoplantar keratoderma due to the KRT1 mutation p.lle479Thr.Semantic proximity Read ↗

[Pathological features and gene mutation analysis in two pedigrees of diffuse palmoplantar keratoderma].Semantic proximity Read ↗

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