Haemochromatosis gene mutation in hepatocellular cancer
Author:
Publisher
Elsevier BV
Subject
General Medicine
Reference5 articles.
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2. A novel MHC class-I like gene is mutated in patients with hereditary haemochromatosis;Feder;Nat Genet,1996
3. A high prevalence of HLA-H 845A mutations in hemochromatosis patients and the normal population in eastern England;Willis;Blood Cells Mol Dis,1997
4. Global prevalence of putative haemochromatosis mutations;Merryweather-Clarke;J Med Genet,1997
5. Norwich and District: on the state of its health;Walker,1990
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1. BolA family member 2 enhances cell proliferation and predicts a poor prognosis in hepatocellular carcinoma with tumor hemorrhage;Journal of Cancer;2019
2. Clinical burden of liver disease from hemochromatosis at an academic medical center;Hepatology Communications;2017-05-18
3. Etiology and Pathogenesis of Hepatocellular Carcinoma: Hepatocellular Carcinoma Associated with Inborn Errors of Metabolism and Hepatobiliary Malformations;Tumors and Tumor-Like Lesions of the Hepatobiliary Tract;2016-10-20
4. Etiology and Pathogenesis of Hepatocellular Carcinoma: Hepatocellular Carcinoma Associated with Inborn Errors of Metabolism and Hepatobiliary Malformations;Tumors and Tumor-Like Lesions of the Hepatobiliary Tract;2016
5. Iron loading and morbidity among relatives of HFE C282Y homozygotes identified either by population genetic testing or presenting as patients;Gut;2006-04-01
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