A novel SLC39A4 gene mutation in the family of an acrodermatitis enteropathica patient with an unusual presentation

Br J Dermatol. 2008 Sep;159(4):976-8. doi: 10.1111/j.1365-2133.2008.08777.x. Epub 2008 Aug 5.
No abstract available

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acrodermatitis / drug therapy
  • Acrodermatitis / genetics*
  • Acrodermatitis / pathology
  • Adult
  • Cation Transport Proteins / genetics*
  • Female
  • Humans
  • Intestinal Absorption / genetics
  • Intestinal Absorption / physiology
  • Mutation / genetics*
  • Pedigree
  • Zinc / administration & dosage
  • Zinc / deficiency*

Substances

  • Cation Transport Proteins
  • SLC39A4 protein, human
  • Zinc