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Article

Genotype-phenotype associations in filaggrin loss-of-function mutation carriers.

Contact dermatitis - 1 Mar 2013

Landeck Lilla, Visser Maaike, Kezic Sanja, John Swen M

Abstract excerpt

BACKGROUND: Loss-of-function mutations in the filaggrin gene (FLG) have been reported to be associated with specific phenotypic characteristics such as hyperlinearity and keratosis pilaris. OBJECTIVES: To study phenotypic features in patients with occupational irritant contact eczema of the hands in relation to FLG loss-of-function mutations. MATERIALS AND METHODS: In a prospective cohort study, genotype was...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 23421459
DOI: 10.1111/j.1600-0536.2012.02171.x

Genes

FLG

Variants

Provenance

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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Genotype-phenotype associations in filaggrin loss-of-function mutation carriers.PMID 23421459Read ↗

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