Molecular insights into mechanisms of iron transport.

Published

Journal Article (Review)

The past 3 years have witnessed extraordinary progress in our understanding of mammalian iron transport and homeostasis. The first transmembrane iron transporter has been found. Mutations in this protein, in two animal models with iron-transport defects, have helped to define the roles of this protein in vivo. The gene defective in patients with hereditary hemochromatosis has been identified, and much has been learned about the structure and function of its gene product. Finally, our ability to make a molecular diagnosis of hereditary hemochromatosis has called attention to new iron-loading disorders, including African iron overload and juvenile hemochromatosis.

Full Text

Duke Authors

Cited Authors

  • Andrews, NC; Fleming, MD; Levy, JE

Published Date

  • March 1999

Published In

Volume / Issue

  • 6 / 2

Start / End Page

  • 61 - 64

PubMed ID

  • 10088633

Pubmed Central ID

  • 10088633

International Standard Serial Number (ISSN)

  • 1065-6251

Digital Object Identifier (DOI)

  • 10.1097/00062752-199903000-00001

Language

  • eng

Conference Location

  • United States