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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...

Täydet tiedot

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Bibliografiset tiedot
Päätekijät: Fleming, Robert E., Britton, Robert S., Waheed, Abdul, Sly, William S., Bacon, Bruce R.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 2005
Aiheet:
Linkit: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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