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Frequency of Two Common HFE Gene Mutations (C282Y and H63D) in a group of Iranian Patients with Cryptogenic Cirrhosis

30 Oct 2011

Abstract excerpt

: Background: The human HFE gene (a key component of iron homeostasis in humans) is involved in hereditary hemochromatosis, a common autosomal recessive genetic disorder that is characterized by excessive intestinal iron absorption and progressive iron overload.Objectives: In this study, we assessed the frequency of two common forms of hemochromatosis HFE gene mutation (C282Y and H63D) in patients suffering from...

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PMID: 22308152
DOI: 10.5812/kowsar.1735143x.781

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Frequency of Two Common HFE Gene Mutations (C282Y and H63D) in a group of Iranian Patients with Cryptogenic CirrhosisPMID 22308152Read ↗

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