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Article

R162W mutation of keratin 9 in a family with autosomal dominant palmoplantar keratoderma with unique histologic features.

The journal of investigative dermatology. Symposium proceedings - 1 Sept 1999

Mayuzumi N, Shigihara T, Ikeda S, Ogawa H

Abstract excerpt

Recurrent R162W mutation ofkeratin 9 has been reported in multiple families with epidermolytic hyperkeratosis (EHK)-type hereditary palmoplantar keratoderma (PPK). Recently, we have observed a family whose members showed autosomal-dominant PPK with unique histologic features such as rounded, dissociated, and slightly eosinophilic keratinocytes at the middle spinous and granular layers of epidermis, but without...

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Identifiers

PMID: 10536990
DOI: 10.1038/sj.jidsp.5640199

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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