Molecular aspects of iron absorption: Insights into the role of HFE in hemochromatosis
Author:
Publisher
Wiley
Subject
Hepatology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1053/jhep.2002.33466/fullpdf
Reference62 articles.
1. A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis;Feder;Nat Genet,1996
2. HFE gene knockout produces mouse model of hereditary hemochromatosis;Zhou;Proc Natl Acad Sci U S A,1998
3. Crystal structure of the hemochromatosis protein HFE and characterization of its interaction with transferrin receptor;Lebron;Cell,1998
4. The hemochromatosis founder mutation in HLA-H disrupts beta2-microglobulin interaction and cell surface expression;Feder;J Biol Chem,1997
5. Hereditary hemochromatosis: effects of C282Y and H63D mutations on association with beta2-microglobulin, intracellular processing, and cell surface expression of the HFE protein in COS-7 cells;Waheed;Proc Natl Acad Sci U S A,1997
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