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Article

Novel mutation of the KRT 10 gene in a Japanese patient with epidermolytic hyperkeratosis.

The Journal of dermatology - 1 Jan 2012

Makino Teruhiko, Furuichi Megumi, Asano Yukie, Shimizu Tadamichi

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Identifiers

PMID: 21463361
DOI: 10.1111/j.1346-8138.2011.01234.x

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Related research

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Research trail→

Click a neighbor to travelStep 1 · 12 closest

Novel mutation of the KRT 10 gene in a Japanese patient with epidermolytic hyperkeratosis.PMID 21463361Read ↗

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

Heterozygous KRT10 missense variant in a Chihuahua with severe epidermolytic ichthyosis.Semantic proximity Read ↗

Splice site and deletion mutations in keratin (KRT1 and KRT10) genes: unusual phenotypic alterations in Scandinavian patients 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 ↗

A novel KRT14 null mutation leads to autosomal recessive epidermolysis bullosa simplex.Semantic proximity Read ↗

A case of epidermolytic ichthyosis showing a very mild phenotype due to a novel tail extension mutation in KRT10.Semantic proximity Read ↗

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

Novel de novo mutation in KRT14 underlies a localized form of epidermolysis bullosa simplex.Semantic proximity Read ↗

In-frame Exon Skipping in KRT5 due to Novel Intronic Deletion Causes Epidermolysis Bullosa Simplex, Generalized Severe.Semantic proximity Read ↗

New KRT10 gene mutation underlying the annular variant of bullous congenital ichthyosiform erythroderma with clinical worsening during pregnancy.Semantic proximity Read ↗

A novel mutation of keratin 9 gene (R162P) in a Japanese family with epidermolytic palmoplantar keratoderma.Semantic proximity Read ↗

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