Mutations and polymorphisms associated with iron overload in a series of 91 non-HFE haemochromatosis patients
Author:
Publisher
Elsevier BV
Subject
Gastroenterology,Hepatology
Reference9 articles.
1. Haemochromatosis;Powell;Lancet,2016
2. Hepcidin and iron homeostasis;Ganz;Biochim Biophys Acta,2012
3. Common conditions associated with hereditary haemochromatosis genetic variants: cohort study in UK Biobank;Pilling;BMJ,2019
4. Iron overload in human disease;Fleming;N Engl J Med,2012
5. A coding polymorphism in the BMP2 gene is associated with iron overload in non-HFE haemochromatosis patients;Lamoril;Blood Cells Mol Dis,2015
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1. Hereditary haemochromatosis: Prevalence and characterization of the disease in a tertiary hospital in Aragon;Medicina Clínica;2024-07
2. Investigation of BMP6 mutations in Brazilian patients with iron overload;Hematology, Transfusion and Cell Therapy;2024-04
3. Severe iron overload in a woman with homeostatic iron regulator ( HFE ) and a novel 5ʹ‐aminolevulinate synthase 2 (ALAS2 ) mutations: interactions of multiple genetic determinants;British Journal of Haematology;2021-09-06
4. Genetic Diagnosis in Hereditary Hemochromatosis: Discovering and Understanding the Biological Relevance of Variants;Clinical Chemistry;2021-08-17
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