Prevalence of FLG loss‐of‐function mutations R501X, 2282del4, and R2447X in Spanish children with atopic dermatitis-Reference-Cited by-同舟云学术

Prevalence of FLG loss‐of‐function mutations R501X, 2282del4, and R2447X in Spanish children with atopic dermatitis

Published:2019-10-21 Issue:1 Volume:37 Page:98-102
ISSN:0736-8046
Container-title:Pediatric Dermatology
language:en
Short-container-title:Pediatr Dermatol

Author:

González‐Tarancón Ricardo¹^ORCID,Sanmartín Rosalia²,Lorente Fabiola¹,Salvador‐Rupérez Elvira¹,Hernández‐Martín Angela³,Rello Luis¹,Puzo Jose¹,Gilaberte Yolanda⁴

Affiliation:

1. Department of Clinical Biochemistry University Hospital Miguel Servet Zaragoza Spain

2. Emergency Unit Salud Huesca Spain

3. Department of Dermatology University Hospital Niño Jesús Madrid Spain

4. Department Dermatology University Hospital Miguel Servet Zaragoza Spain

Publisher

Wiley

Subject

Dermatology,Pediatrics, Perinatology, and Child Health

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/pde.14025

Reference22 articles.

1. 2014 update on atopic dermatitis in children

2. One Remarkable Molecule: Filaggrin

3. Filaggrin Genotype in Ichthyosis Vulgaris Predicts Abnormalities in Epidermal Structure and Function

4. Common loss-of-function variants of the epidermal barrier protein filaggrin are a major predisposing factor for atopic dermatitis

5. Ichthyosis vulgaris: the filaggrin mutation disease

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