Clinical haemochromatosis in HFE mutation carriers

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Presentation transcript:

Clinical haemochromatosis in HFE mutation carriers Ernest Beutler, Vincent Felitti, James A Koziol, Terri Gelbart The Lancet Volume 360, Issue 9330, Pages 413-414 (August 2002) DOI: 10.1016/S0140-6736(02)09584-3 Copyright © 2002 Elsevier Ltd Terms and Conditions

Figure Symptoms of all C282Y/C282Y homozygotes with compound heterozygotes and wild-type homozygotes AST=aspartate aminotransferase. Bars=1 SE. The Lancet 2002 360, 413-414DOI: (10.1016/S0140-6736(02)09584-3) Copyright © 2002 Elsevier Ltd Terms and Conditions