MutantHFE genotype leads to significant iron overload in patients with liver diseases from western Romania-Reference-Cited by-同舟云学术

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MutantHFE genotype leads to significant iron overload in patients with liver diseases from western Romania

Published:2009-06 Issue:2 Volume:50 Page:173-176
ISSN:1234-1983
Container-title:Journal of Applied Genetics
language:en
Short-container-title:J Appl Genet

Author:

Neghina A. -M.,Anghel A.,Sporea I.,Popescu A.,Neghina R.,Collins A.,Thorstensen K.

Publisher

Springer Science and Business Media LLC

Subject

Genetics,General Medicine

Link

http://link.springer.com/content/pdf/10.1007/BF03195670.pdf

Reference10 articles.

1. Adams PC, Reboussin DM, Press RD, Barton JC, Acton RT, Moses GC, et al. 2007. Biological Variability of Transferrin Saturation and Unsaturated Iron-Binding Capacity. Am J Med 120: 999.e1–999.e7.

2. Bollhalder M, Mura C, Landt O, Maly FE, 1999. LightCycler PCR assay for simultaneous detection of the H63D and S65C mutations in theHFE hemochromatosis gene based on opposite melting temperature shifts. Clin Chem 45: 2275–2278.

3. Brissot P, Troadec MB, Bardou-Jacquet E, Le Lan C, Jouanolle AM, Deugnier Y, et al. 2008. Current approach to hemochromatosis. Blood Rev 22: 195–210.

4. Ellervik C, Birgens H, Tybjćrg-Hansen A, Nordestgaard BG, 2007. Hemochromatosis genotypes and risk of 31 disease endpoints: meta-analyses including 66,000 cases and 226,000 controls. Hepatology 46: 1071–1080.

5. Feder JN, Gnirke A, Thomas W, Tsuchihashi Z, Ruddy DA, Basava A, et al. 1996. Anovel MHC class I-like gene is mutated in patients with hereditary haemochromatosis. Nat Genet 13: 399–408.

Cited by 5 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Association between the HFE C282Y, H63D Polymorphisms and the Risks of Non-Alcoholic Fatty Liver Disease, Liver Cirrhosis and Hepatocellular Carcinoma: An Updated Systematic Review and Meta-Analysis of 5,758 Cases and 14,741 Controls;PLOS ONE;2016-09-22

2. Frequency of Two Common HFE Gene Mutations (C282Y and H63D) in a Group of Iranian Patients With Cryptogenic Cirrhosis;Hepatitis Monthly;2011-11-01

3. Frequency of Two Common HFE Gene Mutations (C282Y and H63D) in a group of Iranian Patients with Cryptogenic Cirrhosis;Hepatitis Monthly;2011-10-30

4. Low frequency of HFE gene mutations in Croatian patients suspected of having hereditary hemochromatosis;Medical Science Monitor;2011

5. Hereditary Hemochromatosis: Awareness and Genetic Testing Acceptability in Western Romania;Genetic Testing and Molecular Biomarkers;2010-12

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