Hemochromatosis: New Insights in Pathogenesis and Diagnosis Following the Discovery of the Gene
Author:
Publisher
Informa UK Limited
Subject
Biochemistry, medical,Clinical Biochemistry,General Biochemistry, Genetics and Molecular Biology
Link
http://www.tandfonline.com/doi/pdf/10.1080/10408369891234200
Reference82 articles.
1. A novel MHC class I–like gene is mutated in patients with hereditary haemochromatosis
2. Global prevalence of putative haemochromatosis mutations.
3. Microcytic anaemia mice have a mutation in Nramp2, a candidate iron transporter gene
4. Cloning and characterization of a mammalian proton-coupled metal-ion transporter
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1. EMQN best practice guidelines for the molecular genetic diagnosis of hereditary hemochromatosis (HH);European Journal of Human Genetics;2015-07-08
2. Spondias pinnata stem bark extract lessens iron overloaded liver toxicity due to hemosiderosis in Swiss albino mice;Annals of Hepatology;2013-01
3. Analysis of HFE gene mutations and HLA-A alleles in Brazilian patients with iron overload;Sao Paulo Medical Journal;2006
4. Role of Liver Biopsy in the Diagnosis of Hepatic Iron Overload in the Era of Genetic Testing;American Journal of Clinical Pathology;2002-07
5. Hemochromatosis Protein (HFE);Wiley Encyclopedia of Molecular Medicine;2002-01-15
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