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Article

A novel keratin 5 mutation in a familial cluster.

Dermatology online journal - 15 Jun 2012

Lev-Tov Hadar, Sivamani Raja K, Burrall Barbara

Abstract excerpt

We report a case of epidermolysis bullosa simplex (EBS) associated with a family cluster of EBS and a novel KRT5 mutation. The case is presented in the context of recent advances in the study of the disease.

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Source

Identifiers

PMID: 22747925

Genes

KRT5

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-22747925-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

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