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Rare HFE variants are the most frequent cause of hemochromatosis in non-c282y homozygous patients with hemochromatosis.
- Published in:
- American Journal of Hematology, 2016, v. 91, n. 12, p. 1202, doi. 10.1002/ajh.24535
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- Article
Monoclonal anti-transferrin antibody: A paradigm for better understanding of iron metabolism.
- Published in:
- American Journal of Hematology, 2015, v. 90, n. 6, p. E129, doi. 10.1002/ajh.24004
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- Article
Polymorphisms in the HFE Gene.
- Published in:
- Human Heredity, 1999, v. 49, n. 1, p. 21, doi. 10.1159/000022835
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- Article
Gender-specific phenotypic expression and screening strategies in C282Y-linked haemochromatosis: a study of 9396 French people.
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- British Journal of Haematology, 2002, v. 118, n. 4, p. 1170, doi. 10.1046/j.1365-2141.2002.03718.x
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- Article
Variable age of onset and clinical severity in transferrin receptor 2 related haemochromatosis: novel observations.
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- British Journal of Haematology, 2013, v. 162, n. 2, p. 278, doi. 10.1111/bjh.12350
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- Article
Polymorphism in intron 4 of HFE does not compromise haemochromatosis mutation results.
- Published in:
- Nature Genetics, 1999, v. 23, n. 3, p. 271, doi. 10.1038/15452
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- Article
Ferroportin Diseases: Functional Studies, a Link Between Genetic and Clinical Phenotype.
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- Human Mutation, 2013, v. 34, n. 11, p. 1529, doi. 10.1002/humu.22396
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- Article
Localization of seven new genes around the HLA-A locus.
- Published in:
- Human Molecular Genetics, 1993, v. 2, n. 1, p. 55
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- Article