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Article

Intragenic Copy Number Variation in the Filaggrin Gene in Ethiopian Patients with Atopic Dermatitis.

Pediatric dermatology - 1 May 2017

Fernandez Kerstin, Asad Samina, Taylan Fulya, Wahlgren Carl-Fredrik, Bilcha Kassahun D, Nordenskjöld Magnus, Winge Mårten C G, Bradley Maria

Abstract excerpt

Genetic variants in filaggrin (FLG) involving truncating mutations or intragenic copy number variation are strongly associated with the risk of developing atopic dermatitis (AD) in European and Asian populations. Few loss-of-function mutations have been identified in Africans, although an association between FLG copy number variation and AD severity in a small African American cohort has been proposed. We studied...

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Source

Identifiers

PMID: 28295514
DOI: 10.1111/pde.13095

Genes

FLG

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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Intragenic Copy Number Variation in the Filaggrin Gene in Ethiopian Patients with Atopic Dermatitis.PMID 28295514Read ↗

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