Identification of a Novel Mutation in the SLC39A4 Gene in a Case of Acrodermatitis Enteropathica. [electronic resource]
- Acta dermato-venereologica Mar 2016
- 424-5 p. digital
Publication Type: Case Reports; Journal Article
1651-2057
10.2340/00015555-2240 doi
Acrodermatitis--diagnosis Cation Transport Proteins--genetics DNA Mutational Analysis Dietary Supplements Female Genetic Predisposition to Disease Heterozygote Humans Infant Mutation Phenotype Skin--drug effects Treatment Outcome Zinc--deficiency