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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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- Journal of Investigative Dermatology, 2006, v. 126, n. 8, p. 1770, doi. 10.1038/sj.jid.5700459
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- Article
Mutation S233L in the 1B Domain of Keratin 1 Causes Epidermolytic Palmoplantar Keratoderma with “Tonotubular” Keratin.
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- Journal of Investigative Dermatology, 2006, v. 126, n. 3, p. 607, doi. 10.1038/sj.jid.5700152
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- Article
Two Cases of Primarily Palmoplantar Keratoderma Associated with Novel Mutations in Keratin 1.
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- Journal of Investigative Dermatology, 2002, v. 119, n. 4, p. 966, doi. 10.1046/j.1523-1747.2002.00186.x
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- Article
Comprehensive analysis of the gene encoding filaggrin uncovers prevalent and rare mutations in ichthyosis vulgaris and atopic eczema.
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- Nature Genetics, 2007, v. 39, n. 5, p. 650, doi. 10.1038/ng2020
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- Article
Common loss-of-function variants of the epidermal barrier protein filaggrin are a major predisposing factor for atopic dermatitis.
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- Nature Genetics, 2006, v. 38, n. 4, p. 441, doi. 10.1038/ng1767
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- Article
Loss-of-function mutations in the gene encoding filaggrin cause ichthyosis vulgaris.
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- Nature Genetics, 2006, v. 38, n. 3, p. 337, doi. 10.1038/ng1743
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- Article
Filaggrin Null Alleles Are Not Associated with Psoriasis.
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- Journal of Investigative Dermatology, 2007, v. 127, n. 8, p. 1878, doi. 10.1038/sj.jid.5700817
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- Article