Common loss-of-function variants of the epidermal barrier protein filaggrin are a major predisposing factor for atopic dermatitis
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Analysis of four prevalent filaggrin mutations (R501X, 2282del4, R2447X and S3247X) in Austrian and German patients with atopic dermatitis
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A common variant on chromosome 11q13.5 is associated with atopic dermatitis
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Molecular identification and expression analysis of filaggrin-2, a member of the S100 fused-type protein family
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Identification of human hornerin and its expression in regenerating and psoriatic skin
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The eczema risk variant on chromosome 11q13 (rs7927894) in the population-based ALSPAC cohort: A novel susceptibility factor for asthma and hay fever
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