A Study of Genes That May Modulate the Expression of Hereditary Hemochromatosis: Transferrin Receptor-1, Ferroportin, Ceruloplasmin, Ferritin Light and Heavy Chains, Iron Regulatory Proteins (IRP)-1 and -2, and Hepcidin
Authors:
- Pauline L. LeePLPauline L. Lee
- Terri GelbartTGTerri Gelbart
- Carol WestCWCarol West
- Carol HalloranCHCarol Halloran
- Vincent FelittiVFVincent Felitti
- Ernest BeutlerEBErnest Beutler
- 1 September 2001
- journal article
- Published by Elsevier in Blood Cells, Molecules, and Diseases
- Vol. 27 (5) , 783-802
Abstract
No abstract availableKeywords
This publication has 19 references indexed in Scilit:
- A mutation in SLC11A3 is associated with autosomal dominant hemochromatosisNature Genetics, 2001
- A Mutation, in the Iron-Responsive Element of H Ferritin mRNA, Causing Autosomal Dominant Iron OverloadThe American Journal of Human Genetics, 2001
- New mutations inactivating transferrin receptor 2 in hemochromatosis type 3Blood, 2001
- Transferrin Receptor-2 Gene and Non-C282Y Homozygous Patients with HemochromatosisBlood Cells, Molecules, and Diseases, 2001
- Mutation Analysis of the Transferrin Receptor-2 Gene in Patients with Iron OverloadBlood Cells, Molecules, and Diseases, 2001
- Transferrin Receptor-2 (TFR2) Mutation Y250X in Alabama Caucasian and African American Subjects with and without Primary Iron OverloadBlood Cells, Molecules, and Diseases, 2001
- The Effect of HFE Genotypes on Measurements of Iron Overload in Patients Attending a Health Appraisal ClinicAnnals of Internal Medicine, 2000
- The gene TFR2 is mutated in a new type of haemochromatosis mapping to 7q22Nature Genetics, 2000
- Incidence of liver disease in people with HFE mutations: Table 1Gut, 2000
- Haemochromatosis gene C282Y homozygotes in an elderly male populationThe Lancet, 1999