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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Egile Nagusiak: E. E. Varlamov, M. K. Tagirova, E. G. Komova, M. A. Prasolova, M. K. Ivanov, V. S. Sukhorukov, A. N. Pampura
Formatua: Artigo
Hizkuntza:Russo
Argitaratua: Ltd. “The National Academy of Pediatric Science and Innovation” 2016-03-01
Saila:Rossijskij Vestnik Perinatologii i Pediatrii
Gaiak:
children
atopic dermatitis
protein filaggrin
flg gene
Sarrera elektronikoa:https://www.ped-perinatology.ru/jour/article/view/102
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