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Article

A recurrent keratin 14 mutation in Dowling-Meara epidermolysis bullosa simplex.

The British journal of dermatology - 1 Oct 1999

Sasaki Y, Shimizu H, Akiyama M, Hiraoka Y, Takizawa Y, Yamada S, Morishima Y, Yamanishi K, Aiso S, Nishikawa T

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 10583131
DOI: 10.1046/j.1365-2133.1999.03124.x

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A recurrent keratin 14 mutation in Dowling-Meara epidermolysis bullosa simplex.PMID 10583131Read ↗

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

A mutation in exon 1 of keratin 14 resulting in a Chinese family with epidermolysis bullosa simplex Dowling-Meara.Semantic proximity Read ↗

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Epidermolysis Bullosa Simplex (Dowling-Meara Type) Is a Genetic Disease Characterized by an Abnormal Keratin-Filament Network Involving Keratins K5 and K14Semantic proximity Read ↗

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

A missense mutation in the rod domain of keratin 14 associated with recessive epidermolysis bullosa simplexSemantic proximity Read ↗

A keratin K14 gene mutation in a Japanese patient with the Dowling-Meara type of epidermolysis bullosa simplex.Semantic proximity Read ↗

A keratin 14 mutational hot spot for epidermolysis bullosa simplex, Dowling-Meara: implications for diagnosis.Semantic proximity Read ↗

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Novel and recurrent mutations in Keratin 5 and 14 in Korean patients with Epidermolysis bullosa simplex.Semantic proximity Read ↗

Genetic analysis of a severe case of Dowling-Meara epidermolysis bullosa simplex.Semantic proximity Read ↗

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