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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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| Asıl Yazarlar: | , , , , , , |
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| Materyal Türü: | Artigo |
| Dil: | Russo |
| Baskı/Yayın Bilgisi: |
Ltd. “The National Academy of Pediatric Science and Innovation”
2016-03-01
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| Seri Bilgileri: | Rossijskij Vestnik Perinatologii i Pediatrii |
| Konular: | |
| Online Erişim: | https://www.ped-perinatology.ru/jour/article/view/102 |
| Etiketler: |
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