The molecular basis of ferroportin-linked hemochromatosis

Mutations in the iron exporter ferroportin (Fpn) (IREG1, SLC40A1, and MTP1) result in hemochromatosis type IV, a disorder with a dominant genetic pattern of inheritance and heterogeneous clinical presentation. Most patients develop iron loading of Kupffer cells with relatively low saturation of plas...

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Bibliografiska uppgifter
Huvudupphovsmän: De Domenico, Ivana, Ward, Diane McVey, Nemeth, Elizabeta, Vaughn, Michael B., Musci, Giovanni, Ganz, Tomas, Kaplan, Jerry
Materialtyp: Artigo
Språk:Inglês
Publicerad: National Academy of Sciences 2005
Ämnen:
Biological Sciences
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC1157058/
https://ncbi.nlm.nih.gov/pubmed/15956209
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.0503804102
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