Filaggrin Gene Mutation c.3321delA is Associated with Dry Phenotypes of Atopic Dermatitis in the Chinese Han Population

Chin Med J (Engl). 2016 Jun 20;129(12):1498-500. doi: 10.4103/0366-6999.183424.
No abstract available

MeSH terms

  • Adolescent
  • Adult
  • Asian People
  • Child
  • Child, Preschool
  • Dermatitis, Atopic / genetics*
  • Female
  • Filaggrin Proteins
  • Genetic Predisposition to Disease
  • Humans
  • Infant
  • Intermediate Filament Proteins / genetics*
  • Male
  • Mutation
  • Young Adult

Substances

  • FLG protein, human
  • Filaggrin Proteins
  • Intermediate Filament Proteins