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Pathophysiology of Hereditary Hemochromatosis

Hereditary hemochromatosis (HH) encompasses several inherited disorders of iron homeostasis characterized by increased gastrointestinal iron absorption and tissue iron deposition. The most common form of this disorder is HFE-related HH, nearly always caused by homozygosity for the C282Y mutation. A...

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Bibliografische gegevens
Hoofdauteurs: Fleming, Robert E., Britton, Robert S., Waheed, Abdul, Sly, William S., Bacon, Bruce R.
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: 2005
Onderwerpen:
Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC2587012/
https://ncbi.nlm.nih.gov/pubmed/16315135
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1055/s-2005-923313
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