H63D homozygotes with hyperferritinaemia: is this genotype, the primary cause of iron overload?
Author:
Publisher
Wiley
Subject
Hematology,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1600-0609.2006.00775.x/fullpdf
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1. Changing Concepts of Haemochromatosis
2. A novel MHC class I–like gene is mutated in patients with hereditary haemochromatosis
3. The hemochromatosis gene product complexes with the transferrin receptor and lowers its affinity for ligand binding
4. Complete Scanning of the Hereditary Hemochromatosis Gene (HFE) by Use of Denaturing HPLC
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