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The Molecular Pathogenesis of Hereditary Hemochromatosis

1 Aug 2011

Abstract excerpt

Hereditary hemochromatosis is a genetic disorder of iron overload. Over the past 15 years, significant advances have been made in understanding the molecular pathogenesis of this disorder. First, genetic studies linked this disorder to mutations in several genes, including HFE, transferrin receptor 2 ( TFR2), hepcidin ( HAMP), ferroportin ( SLC40A1), and hemojuvelin ( HFE2). Recent progress has generated...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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PMID: 21901658
DOI: 10.1055/s-0031-1286059

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