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Exome Sequencing and Rare Variant Analysis Reveals Multiple Filaggrin Mutations in Bangladeshi Families with Atopic Eczema and Additional Risk Genes

29 May 2018

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PMID: 29857066
DOI: 10.1016/j.jid.2018.05.013

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Exome Sequencing and Rare Variant Analysis Reveals Multiple Filaggrin Mutations in Bangladeshi Families with Atopic Eczema and Additional Risk GenesPMID 29857066Read ↗

Exome Sequencing of Filaggrin and Related Genes in African-American Children with Atopic DermatitisSemantic proximity Read ↗

Filaggrin's fuller figure: a glimpse into the genetic architecture of atopic dermatitis.Semantic proximity Read ↗

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[Filaggrin gene mutations are frequent and increase the risk of skin disease].Semantic proximity Read ↗

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

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

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

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Trying to understand the genetics of atopic dermatitis.Semantic proximity Read ↗

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

Filaggrin mutations in early- and late-onset atopic dermatitis.Semantic proximity Read ↗

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