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Article

Whole-exome sequencing identifies novel autosomal recessive DSG1 mutations associated with mild SAM syndrome.

The British journal of dermatology - 1 Feb 2016

Schlipf N A, Vahlquist A, Teigen N, Virtanen M, Dragomir A, Fismen S, Barenboim M, Manke T, Rösler B, Zimmer A, Fischer J

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Topics

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Share to Dermatitis
Share to Desmoglein 1
Share to Exome
Share to Genes, Recessive

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Hypersensitivity

Share to Keratoderma, Palmoplantar

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Source

Identifiers

PMID: 26288349
DOI: 10.1111/bjd.14079

Genes

DSG1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

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