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Long-term sequelae of HFE deletion in C57BL/6 × 129/O1a mice, an animal model for hereditary haemochromatosis

  • Published:2002-08 Issue:8 Volume:32 Page:603-612
  • ISSN:0014-2972
  • Container-title:European Journal of Clinical Investigation
  • language:en
  • Short-container-title:

Author:

Lebeau A.,Frank J.,Biesalski H. K.,Weiss G.,Srai S. K. S.,Simpson R. J.,McKie A. T.,Bahram S.,Gilfillan S.,Schümann K.

Publisher

Wiley

Subject

Clinical Biochemistry,Biochemistry,General Medicine

Reference41 articles.

1. A novel MHC class 1-like gene is mutated in patients with hereditary hemochromatosis;Feder;Nature Genet,1996

2. Iron overload: molecular clues to its causes;Kühn;TIBS,1999

3. Hereditary hemochromatosis; Detecting and correcting iron overload;Olynyk;Postgrad Med,1994

4. Value of hepatic iron measurements in early hemochromatosis and determination of the critical iron level associated with fibrosis;Bassett;Hepatology,1986

5. Hereditary hemochromatosis: etiologic, pathologic and clinical aspects;Bothwell;Sem Hematol,1998

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