Cargando…
Chromosome 11q13.5 variant associated with childhood eczema: An effect supplementary to filaggrin mutations
BACKGROUND: Atopic eczema is a common inflammatory skin disease with multifactorial etiology. The genetic basis is incompletely understood; however, loss of function mutations in the filaggrin gene (FLG) are the most significant and widely replicated genetic risk factor reported to date. The first g...
| Autores principales: | , , , , , |
|---|---|
| Formato: | Texto |
| Lenguaje: | English |
| Publicado: |
Mosby
2010
|
| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3038266/ https://www.ncbi.nlm.nih.gov/pubmed/20109745 http://dx.doi.org/10.1016/j.jaci.2009.10.046 |