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Article

Epidermolysis Bullosa Simplex (Dowling-Meara Type) Is a Genetic Disease Characterized by an Abnormal Keratin-Filament Network Involving Keratins K5 and K14

1 Dec 1991

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 1721080
DOI: 10.1111/1523-1747.ep12491885

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Related research

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Click a neighbor to travelStep 1 · 12 closest

Epidermolysis Bullosa Simplex (Dowling-Meara Type) Is a Genetic Disease Characterized by an Abnormal Keratin-Filament Network Involving Keratins K5 and K14PMID 1721080Read ↗

Keratins and epidermolysis bullosa simplexSemantic proximity Read ↗

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

Epidermolysis bullosa simplex in Scotland caused by a spectrum of keratin mutations.Semantic proximity Read ↗

Novel keratin 5 and 14 gene mutations in patients with epidermolysis bullosa simplex from Poland.Semantic proximity Read ↗

Pathological Mechanisms Involved in Epidermolysis Bullosa Simplex: Current Knowledge and Therapeutic Perspectives.Semantic proximity Read ↗

Epidermolysis bullosa simplex: a paradigm for disorders of tissue fragility.Semantic proximity Read ↗

Mutations in KRT5 and KRT14 cause epidermolysis bullosa simplex in 75% of the patients.Semantic proximity Read ↗

A novel keratin K5 gene mutation in Dowling-Meara epidermolysis bullosa simplex.Semantic proximity Read ↗

Identification of novel and known mutations in the genes for keratin 5 and 14 in Danish patients with epidermolysis bullosa simplex: correlation between genotype and phenotype.Semantic proximity Read ↗

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

Verrucous carcinoma in epidermolysis bullosa simplex is possibly associated with a novel mutation in the keratin 5 gene.Semantic proximity Read ↗

Human keratin diseases: the increasing spectrum of disease and subtlety of the phenotype-genotype correlation.Semantic proximity Read ↗

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