Down-regulation of hepcidin in porphyria cutanea tarda

Hepatic siderosis is common in patients with porphyria cutanea tarda (PCT). Mutations in the hereditary hemochromatosis (hh) gene (HFE) explain the siderosis in approximately 20% patients, suggesting that the remaining occurrences result from additional genetic and environmental factors. Two genes k...

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Bibliografiska uppgifter
Huvudupphovsmän: Ajioka, Richard S., Phillips, John D., Weiss, Robert B., Dunn, Diane M., Smit, Maria W., Proll, Sean C., Katze, Michael G., Kushner, James P.
Materialtyp: Artigo
Språk:Inglês
Publicerad: American Society of Hematology 2008
Ämnen:
Red Cells
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC2597139/
https://ncbi.nlm.nih.gov/pubmed/18809758
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1182/blood-2008-02-138222
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