Tumor necrosis factor α promoter polymorphisms and liver abnormalities of homozygotes for the 845G>A (C282Y) hereditary hemochromatosis mutation [3]

Blood

Volumn 100, Issue 6, 2002, Pages 2268-2269

  Beutler, Ernest ^a   Gelbart, Terri ^a  

^a SCRIPPS RESEARCH INSTITUTE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ASPARTATE AMINOTRANSFERASE; COLLAGEN TYPE 4; FERRITIN; TUMOR NECROSIS FACTOR ALPHA;

GENE MUTATION; GENETIC POLYMORPHISM; GENETIC RISK; GENOTYPE; HEMOCHROMATOSIS; HOMOZYGOTE; HUMAN; LETTER; LIVER INJURY; PHENOTYPE; PRIORITY JOURNAL; PROMOTER REGION; RISK FACTOR;

EID: 0037105548     PISSN: 00064971     EISSN: None     Source Type: Journal    
DOI: 10.1182/blood-2002-05-1520     Document Type: Letter

References (3)

1. Penetrance of the 845G→A (C282Y) HFE hereditary hemochromatosis mutation
2. Tumor necrosis factor alpha promoter polymorphisms influence the phenotypic expression of hereditary hemochromatosis
3. Elevated serum type IV collagen: A sensitive indicator of the presence of cirrhosis in haemochromatosis