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John E. A. Common et al.
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FLG mutation p.Lys4021X in the C-terminal imperfect filaggrin repeat in Japanese patients with atopic eczema
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Filaggrin gene defects and risk of developing allergic sensitisation and allergic disorders: systematic review and meta-analysis
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Filaggrin null mutations and childhood atopic eczema: A population-based case-control study
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De novo occurrence of the filaggrin mutation p.R501X with prevalent mutation c.3321delA in a Japanese family with ichthyosis vulgaris complicated by atopic dermatitis
Takahiro Hamada et al.
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Prevalent and low-frequency null mutations in the filaggrin gene are associated with early-onset and persistent atopic eczema
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Unique and recurrent mutations in the filaggrin gene in Singaporean Chinese patients with ichthyosis vulgaris
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Specific filaggrin mutations cause ichthyosis vulgaris and are significantly associated with atopic dermatitis in Japan
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SEMINARS IN CUTANEOUS MEDICINE AND SURGERY (2008)
Filaggrin mutations are genetic modifying factors exacerbating X-linked ichthyosis
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Filaggrin mutations in children with severe atopic dermatitis
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Null mutations in the filaggrin gene (FLG) determine major susceptibility to early-onset atopic dermatitis that persists into adulthood
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Unique mutations in the filaggrin gene in Japanese patients with ichthyosis vulgaris and atopic dermatitis
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Filaggrin loss-of-function variant contributes to atopic dermatitis risk in the population of Northern Germany
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Filaggrin loss-of-function mutations predispose to phenotypes involved in the atopic march
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Prevalent and rare mutations in the gene encoding filaggrin cause ichthyosis vulgaris and predispose individuals to atopic dermatitis
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Loss-of-function variations within the filaggrin gene predispose for atopic dermatitis with allergic sensitizations
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Common loss-of-function variants of the epidermal barrier protein filaggrin are a major predisposing factor for atopic dermatitis
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Loss-of-function mutations in the gene encoding filaggrin cause ichthyosis vulgaris
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BRITISH JOURNAL OF DERMATOLOGY (2002)
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