Transferrin receptor-2 gene and non-C282Y homozygous patients with hemochromatosis

Blood Cells, Molecules, and Diseases

Volumn 27, Issue 1, 2001, Pages 290-293

  Aguilar Martinez, Patricia ^a   Esculié Coste, Carole ^a   Bismuth, Michael ^a   Giansily Blaizot, Muriel ^a   Larrey, Dominique ^a   Schved, Jean François ^a  

^a MONTPELLIER UNIVERSITY HOSPITAL   (France)

Author keywords

Hereditary hemochromatosis; Transferrin receptor 2

Indexed keywords

TRANSFERRIN RECEPTOR; TRANSFERRIN RECEPTOR 2; UNCLASSIFIED DRUG;

ADULT; AGED; ARTICLE; CLINICAL ARTICLE; FEMALE; GENE MUTATION; GENE SEQUENCE; GENOTYPE; HEMOCHROMATOSIS; HOMOZYGOSITY; HUMAN; IRON METABOLISM; IRON OVERLOAD; MALE; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; RECEPTOR GENE;

GENETTA; STAPHYLOCOCCUS PHAGE 187;

EID: 0035046454     PISSN: 10799796     EISSN: None     Source Type: Journal    
DOI: 10.1006/bcmd.2001.0382     Document Type: Article

References (11)

1. Evidence that the ancestral haplotype in Australian hemochromatosis patients may be associated with a common mutation in the gene
2. A novel MCH class I-gene is mutated in patients with hereditary hemochromatosis
3. Mutation analysis in hereditary hemochromatosis
4. Haemochromatosis and HLA-H
5. Haemochromatosis and HLA H
6. Compound heterozygotes for hemochromatosis gene mutations: May they help to understand the pathophysiology of the disease?
7. The gene TFR2 is mutated in a new type of haemochromatosis mapping to 7q22
8. Molecular cloning of transferrin receptor 2. A new member of the transferrin receptor-like family
9. Transferrin receptor 2: Continued expression in mouse liver in the face of iron overload and in hereditary hemochromatosis
10. Phenotypic expression of iron overload in 50 H63D homozygotes
11. Genes that modify the hemochromatosis phenotype mice