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Clinical haemochromatosis in HFE mutation carriers

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Presentation on theme: "Clinical haemochromatosis in HFE mutation carriers"— Presentation transcript:

1 Clinical haemochromatosis in HFE mutation carriers
Ernest Beutler, Vincent Felitti, James A Koziol, Terri Gelbart  The Lancet  Volume 360, Issue 9330, Pages (August 2002) DOI: /S (02) Copyright © 2002 Elsevier Ltd Terms and Conditions

2 Figure Symptoms of all C282Y/C282Y homozygotes with compound heterozygotes and wild-type homozygotes AST=aspartate aminotransferase. Bars=1 SE. The Lancet  , DOI: ( /S (02) ) Copyright © 2002 Elsevier Ltd Terms and Conditions


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