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Article

Filaggrin Gene Mutations with Special Reference to Atopic Dermatitis

10 Jul 2020

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 33585163
DOI: 10.1007/s40521-020-00271-x

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Filaggrin Gene Mutations with Special Reference to Atopic DermatitisPMID 33585163Read ↗

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Two Common Loss-of-Function Mutations within the Filaggrin Gene Predispose for Early Onset of Atopic DermatitisSemantic proximity Read ↗

The clinical relevance of filaggrin mutations: Effect on allergic disease.Semantic proximity Read ↗

Common loss-of-function variants of the epidermal barrier protein filaggrin are a major predisposing factor for atopic dermatitisSemantic proximity Read ↗

Filaggrin haploinsufficiency among patients with dermatitis from a tertiary referral centre: early findings and possible phenotype.Semantic proximity Read ↗

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Filaggrin mutations and the skin.Semantic proximity Read ↗

Common filaggrin gene loss-of-function variants are associated with skin cancer risk.Semantic proximity Read ↗

Increased compound heterozygous filaggrin mutations in severe atopic dermatitis in the United States.Semantic proximity Read ↗

Filaggrin loss-of-function mutations and association with allergic diseases.Semantic proximity Read ↗

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