Mutation analysis of the transferrin receptor-2 gene in patients with iron overload

Blood Cells, Molecules, and Diseases

Volumn 27, Issue 1, 2001, Pages 285-289

  Lee, Pauline L ^a   Halloran, Carol ^a   West, Carol ^a   Beutler, Ernest ^a  

^a SCRIPPS RESEARCH INSTITUTE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

FERRITIN; GENE PRODUCT; HFE PROTEIN; IRON; TRANSFERRIN; TRANSFERRIN RECEPTOR; TRANSFERRIN RECEPTOR 2; UNCLASSIFIED DRUG;

ARTICLE; CLINICAL ARTICLE; CONTROLLED STUDY; GENE MUTATION; GENE SEQUENCE; GENETIC POLYMORPHISM; GENOTYPE; HEMOCHROMATOSIS; HUMAN; IRON OVERLOAD; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; RECEPTOR GENE;

PIERINAE;

EID: 0035049344     PISSN: 10799796     EISSN: None     Source Type: Journal    
DOI: 10.1006/bcmd.2001.0381     Document Type: Article

References (5)

1. Molecular cloning of transferrin receptor 2 - A new member of the transferrin receptor-like family
2. Transferrin receptor 2: Continued expression in mouse liver in the face of iron overload and in hereditary hemochromatosis
3. Transferrin receptor is necessary for development of erythrocytes and the nervous system
4. The gene TFR2 is mutated in a new type of haemochromatosis mapping to 7q22
5. The effect of HFE genotypes in patients attending a health appraisal clinic