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Published in: Annals of Hematology 6/2013

01-06-2013 | Letter to the Editor

Molecular basis of primary iron overload in India and the role of serum-derived factors in hepcidin regulation

Authors: Rekha Athiyarath, Alok Srivastava, Eunice Sindhuvi Edison

Published in: Annals of Hematology | Issue 6/2013

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Excerpt

Dear Editor, …
Appendix
Available only for authorised users
Literature
1.
go back to reference 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):86–90PubMedCrossRef 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):86–90PubMedCrossRef
2.
go back to reference 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):2956–2959PubMed 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):2956–2959PubMed
3.
go back to reference 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):166–169PubMedCrossRef 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):166–169PubMedCrossRef
4.
go back to reference Beutler E, West C (1997) New diallelic markers in the HLA region of chromosome 6. Blood Cells Mol Dis 23(2):219–229PubMedCrossRef Beutler E, West C (1997) New diallelic markers in the HLA region of chromosome 6. Blood Cells Mol Dis 23(2):219–229PubMedCrossRef
5.
go back to reference 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):229–232PubMedCrossRef 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):229–232PubMedCrossRef
6.
go back to reference Ravasi G et al (2012) Hepcidin expression in iron overload diseases is variably modulated by circulating factors. PLoS One 7(5):e36425PubMedCrossRef Ravasi G et al (2012) Hepcidin expression in iron overload diseases is variably modulated by circulating factors. PLoS One 7(5):e36425PubMedCrossRef
7.
go back to reference Ramos P et al (2010) Enhanced erythropoiesis in Hfe-KO mice indicates a role for Hfe in the modulation of erythroid iron homeostasis. Blood 117(4):1379–1389PubMedCrossRef Ramos P et al (2010) Enhanced erythropoiesis in Hfe-KO mice indicates a role for Hfe in the modulation of erythroid iron homeostasis. Blood 117(4):1379–1389PubMedCrossRef
8.
go back to reference Jain S et al (2011) Lack of association of primary iron overload and common HFE gene mutations with liver cirrhosis in adult Indian population. Indian J Gastroenterol 30(4):161–165PubMedCrossRef Jain S et al (2011) Lack of association of primary iron overload and common HFE gene mutations with liver cirrhosis in adult Indian population. Indian J Gastroenterol 30(4):161–165PubMedCrossRef
9.
go back to reference Shukla P et al (2006) HFE, hepcidin and ferroportin gene mutations are not present in Indian patients with primary haemochromatosis. Natl Med J India 19(1):20–23PubMed Shukla P et al (2006) HFE, hepcidin and ferroportin gene mutations are not present in Indian patients with primary haemochromatosis. Natl Med J India 19(1):20–23PubMed
Metadata
Title
Molecular basis of primary iron overload in India and the role of serum-derived factors in hepcidin regulation
Authors
Rekha Athiyarath
Alok Srivastava
Eunice Sindhuvi Edison
Publication date
01-06-2013
Publisher
Springer-Verlag
Published in
Annals of Hematology / Issue 6/2013
Print ISSN: 0939-5555
Electronic ISSN: 1432-0584
DOI
https://doi.org/10.1007/s00277-012-1621-0

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