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...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Prif Awduron: E. E. Varlamov, M. K. Tagirova, E. G. Komova, M. A. Prasolova, M. K. Ivanov, V. S. Sukhorukov, A. N. Pampura
Fformat: Artigo
Iaith:Russo
Cyhoeddwyd: Ltd. “The National Academy of Pediatric Science and Innovation” 2016-03-01
Cyfres:Rossijskij Vestnik Perinatologii i Pediatrii
Pynciau:
children
atopic dermatitis
protein filaggrin
flg gene
Mynediad Ar-lein:https://www.ped-perinatology.ru/jour/article/view/102
Tagiau: Ychwanegu Tag
Dim Tagiau, Byddwch y cyntaf i dagio'r cofnod hwn!

Eitemau Tebyg