Mutation analysis of transferrin-receptor 2 in patients with atypical hemochromatosis [5]

Blood

Volumn 100, Issue 3, 2002, Pages 1099-1100

  Hofmann, Wolf K ^a   Tong, Xiang Jun ^a   Ajioka, Richard S ^a   Kushner, James P ^a   Koeffler, H Phillip ^a  

^a UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

GENOMIC DNA; TRANSFERRIN RECEPTOR;

CLINICAL ARTICLE; GENE MUTATION; GENETIC DISORDER; GENETIC POLYMORPHISM; GENOME; HEMOCHROMATOSIS; HUMAN; LETTER; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; SINGLE STRAND CONFORMATION POLYMORPHISM;

EID: 0036682965     PISSN: 00064971     EISSN: None     Source Type: Journal    
DOI: 10.1182/blood-2002-04-1077     Document Type: Letter

References (8)

1. A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis
2. Molecular cloning of transfein receptor 2: A new member of the transfein receptor-like family
3. The gene TFR2 is mutated in a new type of haemochromatosis mapping to 7q22
4. TFR2 Y250X mutation in Italy
5. New mutations inactivating transterrin receptor 2 in hemochromatosis type 3
6. A new mutation in transferrin receptor 2 gene in hemochromatosis type 3
7. Mutation analysis of the DNA-damage checkpoint gene CHK2 in myelodysplastic syndromes and acute myeloid leukemias
8. Transferrin receptor 2: Continued expression in mouse liver in the face of iron overload and in hereditary hemochromatosis