The discovery of the association of FLG mutations with atopic diseases followed insights into a common disorder of keratinization, ichthyosis vulgaris. The epidermis of individuals with AD shows a ...
Recently, the molecular basis of IV was ascribed to loss-of-function mutations in the gene encoding filaggrin (FLG), namely p.R501X and c.2282del4. Homozygotes and compound heterozygotes were ...
Some results have been hidden because they may be inaccessible to you
Show inaccessible results
Feedback