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Article

Autosomal dominant monilethrix with incomplete penetrance due to a novel KRT86 mutation in a Chinese family.

Anais brasileiros de dermatologia - 1 Jan 2024

Dai Ru, Wang Tingting, Wu Xianjie

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Identifiers

PMID: 38594178
DOI: 10.1016/j.abd.2022.12.010
PMCID: PMC11221135

Genes

KRT86

Provenance

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

Related research

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Autosomal dominant monilethrix with incomplete penetrance due to a novel KRT86 mutation in a Chinese family.PMID 38594178Read ↗

Monilethrix in monozygotic twins with very rare mutation in KRT 86 gene.Semantic proximity Read ↗

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A novel KRT86 mutation in a Turkish family with monilethrix, and identification of maternal mosaicism.Semantic proximity Read ↗

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