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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Bibliografski detalji
Glavni autori: E. E. Varlamov, M. K. Tagirova, E. G. Komova, M. A. Prasolova, M. K. Ivanov, V. S. Sukhorukov, A. N. Pampura
Format: Artigo
Jezik:Russo
Izdano: Ltd. “The National Academy of Pediatric Science and Innovation” 2016-03-01
Serija:Rossijskij Vestnik Perinatologii i Pediatrii
Teme:
children
atopic dermatitis
protein filaggrin
flg gene
Online pristup:https://www.ped-perinatology.ru/jour/article/view/102
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