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The HFE Cys282Tyr mutation as a necessary but not sufficient cause of clinical hereditary hemochromatosis.

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Affiliations

  • 1. Department of Molecular and Experimental Medicine, Scripps Research Institute, La Jolla, CA 92037, USA.
      Authors
    • Beutler E 1
    (1 author)

Blood, 01 May 2003, 101(9):3347-3350
https://doi.org/10.1182/blood-2002-06-1747 PMID: 12707220 

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Abstract 

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Read article at publisher's site: https://doi.org/10.1182/blood-2002-06-1747

Read article for free, from open access legal sources, via Unpaywall: https://ashpublications.org/blood/article-pdf/101/9/3347/1255625/h80903003347a.pdfUnpaywall

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Funding 

Funders who supported this work.

NCRR NIH HHS (1)

NIDDK NIH HHS (1)