Abstract
Diverse hereditary disorders associated with iron accumulation cause widespread organ damage. New insights into cellular pathways of iron transport have emerged from the identification of molecules implicated in heritable defects of iron metabolism. Unravelling the genetic basis of rare variants of haemochromatosis should provide vital functional information to further our mechanistic understanding of iron homeostasis.
Publication types
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Research Support, Non-U.S. Gov't
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Review
MeSH terms
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Adult
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Animals
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Child
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HLA Antigens / genetics
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HLA Antigens / metabolism
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Hemochromatosis / genetics*
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Hemochromatosis / pathology
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Hemochromatosis / physiopathology*
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Hemochromatosis Protein
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Histocompatibility Antigens Class I / genetics
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Histocompatibility Antigens Class I / metabolism
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Humans
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Infant
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Infant, Newborn
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Iron / metabolism*
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Membrane Proteins*
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Mice
Substances
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HFE protein, human
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HLA Antigens
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Hemochromatosis Protein
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Hfe protein, mouse
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Histocompatibility Antigens Class I
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Membrane Proteins
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Iron