Compound Heterozygotes for Hemochromatosis Gene Mutations: May They Help to Understand the Pathophysiology of the Disease?-Reference-Cited by-同舟云学术

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Compound Heterozygotes for Hemochromatosis Gene Mutations: May They Help to Understand the Pathophysiology of the Disease?

Published:1997-08 Issue:2 Volume:23 Page:269-276
ISSN:1079-9796
Container-title:Blood Cells, Molecules, and Diseases
language:en
Short-container-title:Blood Cells, Molecules, and Diseases

Author:

Aguilar Martinez Patricia,Biron Christine,Blanc François,Masmejean Christophe,Jeanjean Philippe,Michel Henri,Schved Jean-François

Publisher

Elsevier BV

Subject

Cell Biology,Hematology,Molecular Biology,Molecular Medicine

Reference11 articles.

1. A novel MCH class I- gene is mutated in patients with hereditary hemochromatosis;Feder;Nat Genet,1996

2. Mutation analysis in hereditary hemochromatosis;Beutler;Blood Cells Mol Dis,1996

3. Haemochromatosis and HLA H;Jouanolle;Nat Genet,1996

4. Haemochromatosis and HLA H;Jazwinska;Nat Genet,1996

5. Genetic irony behond haemochromatosis: Clinical effects of HLA-H mutations;Beutler;Lancet,1997

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1. État scléreux révélant une porphyrie cutanée tardive;Annales de Dermatologie et de Vénéréologie;2018-08

2. The H63D Mutation of the Hemochromatosis Gene is Associated with Sustained Virological Response in Chronic Hepatitis C Patients Treated with Interferon-Based Therapy: A Meta-Analysis;The Tohoku Journal of Experimental Medicine;2012

3. The importance of phase information for human genomics;Nature Reviews Genetics;2011-02-08

4. Hemochromatosis Genotypes and Risk of Iron Overload—A Meta-Analysis;Annals of Epidemiology;2011-01

5. EASL clinical practice guidelines for HFE hemochromatosis;Journal of Hepatology;2010-07

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