Molecular basis of primary iron overload in India and the role of serum-derived factors in hepcidin regulation
Author:
Publisher
Springer Science and Business Media LLC
Subject
Hematology,General Medicine
Link
http://link.springer.com/content/pdf/10.1007/s00277-012-1621-0.pdf
Reference9 articles.
1. Thakur V et al (2004) Absence of hemochromatosis associated Cys282Tyr HFE gene mutation and low frequency of hemochromatosis phenotype in non-alcoholic chronic liver disease patients in India. J Gastroenterol Hepatol 19(1):86–90
2. Dhillon BK et al (2007) Frequency of primary iron overload and HFE gene mutations (C282Y, H63D and S65C) in chronic liver disease patients in north India. World J Gastroenterol 13(21):2956–2959
3. Aguilar-Martinez P et al (1999) Haplotype analysis of the HFE gene: implications for the origins of hemochromatosis related mutations. Blood Cells Mol Dis 25(3–4):166–169
4. Beutler E, West C (1997) New diallelic markers in the HLA region of chromosome 6. Blood Cells Mol Dis 23(2):219–229
5. Dhillon BK et al (2012) H63D mutation in HFE gene is common in Indians and is associated with the European haplotype. J Genet 91(2):229–232
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1. Hemochromatosis in India: First Report of Whole Exome Sequencing With Review of the Literature;Journal of Clinical and Experimental Hepatology;2020-03
2. Adult onset hereditary hemochromatosis is associated with a novel recurrent Hemojuvelin (HJV) gene mutation in north Indians;Blood Cells, Molecules, and Diseases;2018-11
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