Human transferrin G277S mutation: A risk factor for iron deficiency anaemia

British Journal of Haematology

Volumn 115, Issue 2, 2001, Pages 329-333

  Lee, Pauline L ^a   Halloran, Carol ^a   Trevino, Renee ^a   Felitti, Vincent ^b   Beutler, Ernest ^a  

^a SCRIPPS RESEARCH INSTITUTE   (United States)

^b KAISER PERMANENTE   (United States)

Author keywords

Haemochromatosis; Iron deficiency anaemia; Mutation; Polymorphism; Transferrin

Indexed keywords

COMPLEMENTARY DNA; IRON; TRANSFERRIN;

ARTICLE; CONTROLLED STUDY; FEMALE; GENE MUTATION; GENOTYPE; HETEROZYGOTE; HOMOZYGOTE; HUMAN; IRON BINDING CAPACITY; IRON DEFICIENCY ANEMIA; MALE; MENSTRUATION; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; RISK FACTOR;

ADULT; AMINO ACID SEQUENCE; ANEMIA, IRON-DEFICIENCY; ANIMALS; FEMALE; GENETIC PREDISPOSITION TO DISEASE; GENOTYPE; HUMANS; IRON; MALE; MIDDLE AGED; POINT MUTATION; POLYMORPHISM, GENETIC; RISK FACTORS; SPECIES SPECIFICITY; TRANSFERRIN;

EID: 0035726009     PISSN: 00071048     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1365-2141.2001.03096.x     Document Type: Article

References (9)

1. DNA polymorphism and haplotypes in the human transferrin gene
2. Molecular characterization of a case of atransferrinemia
3. The effect of HFE genotypes in patients attending a health appraisal clinic
4. The effect of transferrin polymorphisms on iron metabolism
5. Transferrin
6. Variations in human β-globulins
7. Third allele at the serum β-globulin locus in humans
8. The molecular defect in hypotransferrinemic mice