Clinical significance of FLG gene mutations in children with atopic dermatitis

Skin barrier dysfunction due to deficiency of the skin protein filaggrin is one of the factors involved in the pathogenesis of atopic dermatitis. Objective: to determine the clinical significance of 2282 del CAGT, R501X, R2447X, and S3247X mutations in the FLG gene in children with atopic dermatitis...

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Détails bibliographiques
Auteurs principaux: E. E. Varlamov, M. K. Tagirova, E. G. Komova, M. A. Prasolova, M. K. Ivanov, V. S. Sukhorukov, A. N. Pampura
Format: Artigo
Langue:Russo
Publié: Ltd. “The National Academy of Pediatric Science and Innovation” 2016-03-01
Collection:Rossijskij Vestnik Perinatologii i Pediatrii
Sujets:
children
atopic dermatitis
protein filaggrin
flg gene
Accès en ligne:https://www.ped-perinatology.ru/jour/article/view/102
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