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Correspondence

Has Lactoferrin a Role in Hereditary Hemochromatosis?

, (Corresponding author), &
Pages 421-422 | Received 12 Aug 1997, Published online: 13 Jul 2016

References

  • Feder J. N., Gnirke, A. Thomas, W. et al. (1996). A novel MCH class I-like gene is mutated in patients with hereditary haemochromatosis. Nature Genetics, 13, 399–408.
  • Milman, N. (1991). Idiopathic haemochromatosis in Denmark 1950–1985. Clinical, histological and biochemical features in 179 patients and 13 preclinical cases. Dan Med Bull., 38, 385–393.
  • Birgens, H. S. (1991). The interaction of lactoferrin with human monocytes. Dan Med Bull., 38, 244–252.
  • Moguilevsky, N., Masson, P.-L. and Courtoy, P.-J. (1987). Lactoferrin uptake and iron processing into macrophages: a study in familial hemochromatosis. Br. J. Haematol., 66, 129–136.
  • Hegnhøj, J. and Schaffalitzky de Muckadell, O. B. (1985). An enzyme linked immunosorbent assay for measurements of lactoferrin in duodenal aspirates and other biological fluids. Scand J Clin Lab. Invest., 45, 489–495.
  • McAbee, D. D. and Ling, Y. Y. (1997). Iron-loading of cultured adult rat hepatocytes reversibly enhances lactoferrin binding and endocytosis. J. Cell Physiol., 171, 75–86.

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