Ferroportin mutation in autosomal dominant hemochromatosis: loss of function, gain in understanding
AUTOR(ES)
Fleming, Robert E.
FONTE
American Society for Clinical Investigation
ACESSO AO ARTIGO
http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=209411Documentos Relacionados
- Autosomal-dominant hemochrom-atosis is associated with a mutation in the ferroportin (SLC11A3) gene
- Aristapedioid: A Gain of Function, Homeotic Mutation in Drosophila Melanogaster
- Increased p53 mutation load in nontumorous human liver of Wilson disease and hemochromatosis: Oxyradical overload diseases
- HFE hemochromatosis: an overview about therapeutic recommendations
- Hereditary hemochromatosis due to resistance to hepcidin: high hepcidin concentrations in a family with C326S ferroportin mutation