Exacerbation of X-linked ichthyosis phenotype in a female by inheritance of filaggrin and steroid sulfatase mutations. [electronic resource]
Producer: 20120224Description: 159-62 p. digitalISSN:- 1873-569X
- Administration, Cutaneous
- Child
- DNA Mutational Analysis
- Dermatologic Agents -- administration & dosage
- Female
- Filaggrin Proteins
- Gene Deletion
- Genetic Predisposition to Disease
- Heredity
- Heterozygote
- Homozygote
- Humans
- Ichthyosis, X-Linked -- drug therapy
- In Situ Hybridization, Fluorescence
- Intermediate Filament Proteins -- genetics
- Mutation, Missense
- Pedigree
- Phenotype
- Severity of Illness Index
- Skin -- drug effects
- Steryl-Sulfatase -- genetics
No physical items for this record
Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
There are no comments on this title.
Log in to your account to post a comment.