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Article

Mutation in DSG1 causing autosomal dominant striate palmoplantar keratoderma.

The British journal of dermatology - 1 Sept 2009

Zamiri M, Smith F J D, Campbell L E, Tetley L, Eady R A J, Hodgins M B, McLean W H I, Munro C S

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 19558595
DOI: 10.1111/j.1365-2133.2009.09316.x

Genes

DSG1

Provenance

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Related research

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Research trail→

Click a neighbor to travelStep 1 · 12 closest

Mutation in DSG1 causing autosomal dominant striate palmoplantar keratoderma.PMID 19558595Read ↗

Striate palmoplantar keratoderma: Report of a novel DSG1 mutation and atypical clinical manifestations.Semantic proximity Read ↗

Novel mutations in DSG1 causing striate palmoplantar keratoderma.Semantic proximity Read ↗

Striate Palmoplantar Keratoderma Showing Transgrediens in a Patient Harbouring Heterozygous Nonsense Mutations in Both DSG1 and SERPINB7.Semantic proximity Read ↗

Mutations in desmoglein 1 cause diverse inherited palmoplantar keratoderma phenotypes: implications for genetic screening.Semantic proximity Read ↗

Mutations in the desmoglein 1 gene in five Pakistani families with striate palmoplantar keratoderma.Semantic proximity Read ↗

Acantholytic dyskeratotic epidermal naevus and striate palmoplantar keratoderma associated with DSG1 mutation: evidence for segmental type 2 mosaicism.Semantic proximity Read ↗

Diffuse nonepidermolytic palmoplantar keratoderma caused by a recurrent nonsense mutation in DSG1.Semantic proximity Read ↗

New and recurrent AAGAB mutations in punctate palmoplantar keratoderma.Semantic proximity Read ↗

Classifying novel DSG1 variants on disease severity in SAM syndrome and palmoplantar keratoderma.Semantic proximity Read ↗

Phenotypic Variability with SLURP1 Mutations and Diffuse Palmoplantar Keratoderma.Semantic proximity Read ↗

Novel nonsense variants in SLURP1 and DSG1 cause palmoplantar keratoderma in Pakistani familiesSemantic proximity Read ↗

Hereditary palmoplantar keratoderma - phenotypes and mutations in 64 patients.Semantic proximity Read ↗

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