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Article

Prevalent and rare mutations in the gene encoding filaggrin in Japanese patients with ichthyosis vulgaris and atopic dermatitis.

The Journal of investigative dermatology - 1 May 2009

Nomura Toshifumi, Akiyama Masashi, Sandilands Aileen, Nemoto-Hasebe Ikue, Sakai Kaori, Nagasaki Akari, Palmer Colin N A, Smith Frances J D, McLean W H Irwin, Shimizu Hiroshi

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Identifiers

PMID: 19037238
DOI: 10.1038/jid.2008.372

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

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Prevalent and rare mutations in the gene encoding filaggrin in Japanese patients with ichthyosis vulgaris and atopic dermatitis.PMID 19037238Read ↗

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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 DermatitisSemantic proximity Read ↗

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Loss-of-function mutations in the gene encoding filaggrin cause ichthyosis vulgaris.Semantic proximity Read ↗

Filaggrin gene polymorphisms in Iranian ichthyosis vulgaris and atopic dermatitis patientsSemantic proximity Read ↗

Comprehensive analysis of the gene encoding filaggrin uncovers prevalent and rare mutations in ichthyosis vulgaris and atopic eczema.Semantic proximity Read ↗

Specific filaggrin mutations cause ichthyosis vulgaris and are significantly associated with atopic dermatitis in Japan.Semantic proximity Read ↗

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