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Article

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

Journal of the European Academy of Dermatology and Venereology : JEADV - 1 Apr 2009

Wu J W, Xiao S X

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Identifiers

PMID: 18717745
DOI: 10.1111/j.1468-3083.2008.02930.x

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A recurrent keratin 14 mutation in Dowling-Meara epidermolysis bullosa simplex in a Chinese family.PMID 18717745Read ↗

A recurrent keratin 14 mutation in Dowling-Meara epidermolysis bullosa simplex.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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One novel and two recurrent mutations in the keratin 5 gene identified in Chinese patients with epidermolysis bullosa simplex.Semantic proximity Read ↗

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

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

Epidermolysis Bullosa: Two rare case reports of COL7A1 and EBS-GEN SEV KRT14 variants with review of literature.Semantic proximity Read ↗

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

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

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