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Article

Two Common Loss-of-Function Mutations within the Filaggrin Gene Predispose for Early Onset of Atopic Dermatitis

28 Sept 2006

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Share to Allergic Rhinitis and Sensitization
Share to Dermatology and Skin Diseases
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Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 17008875
DOI: 10.1038/sj.jid.5700579

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Related research

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Two Common Loss-of-Function Mutations within the Filaggrin Gene Predispose for Early Onset of Atopic DermatitisPMID 17008875Read ↗

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

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Prevalent and Low-Frequency Null Mutations in the Filaggrin Gene Are Associated with Early-Onset and Persistent Atopic EczemaSemantic proximity Read ↗

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

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

Filaggrin mutations associated with skin and allergic diseases.Semantic proximity Read ↗

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

The role of filaggrin loss-of-function mutations in atopic dermatitis.Semantic proximity Read ↗

Loss-of-function mutations within the filaggrin gene and atopic dermatitis.Semantic proximity Read ↗

Filaggrin Gene Mutations with Special Reference to Atopic DermatitisSemantic proximity Read ↗

Filaggrin mutations and the skin.Semantic proximity Read ↗

Atopic eczema and the filaggrin story.Semantic proximity Read ↗

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