Molecular basis of HFE-hemochromatosis
Iron-overload disorders owing to genetic misregulation of iron acquisition are referred to as hereditary hemochromatosis (HH). The most prevalent genetic iron overload disorder in Caucasians is caused by mutations in the HFE gene, an atypical MHC class I molecule. Recent studies classified HFE/Hfe-h...
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| Format: | Artigo |
| Sprache: | Inglês |
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Frontiers Media S.A.
2014-03-01
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| Schriftenreihe: | Frontiers in Pharmacology |
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| Online-Zugang: | http://journal.frontiersin.org/Journal/10.3389/fphar.2014.00042/full |
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