The hemochromatosis N144H mutation of SLC11A3 gene in patients with type 2 diabetes

Molecular Genetics and Metabolism

Volumn 75, Issue 3, 2002, Pages 290-291

  Njajou, Omer T ^a   Vaessen, Norbert ^a   Oostra, Ben ^a   Heutink, Peter ^a   Van Duijn, Cornelia M ^a  

^a ERASMUS MEDICAL CENTER   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

AUTOSOMAL DOMINANT INHERITANCE; CHROMOSOME 2Q; GENE MUTATION; GENETIC CODE; GENETIC SUSCEPTIBILITY; GLUCOSE TOLERANCE; HEMOCHROMATOSIS; HETEROZYGOSITY; HUMAN; INSULIN RESISTANCE; INTESTINE CELL; IRON STORAGE; IRON TRANSPORT; LETTER; NON INSULIN DEPENDENT DIABETES MELLITUS; OXIDATION; PRIORITY JOURNAL; SCREENING; TRANSFERRIN BLOOD LEVEL;

EID: 0036354775     PISSN: 10967192     EISSN: None     Source Type: Journal    
DOI: 10.1006/mgme.2002.3299     Document Type: Editorial

References (5)

1. A mutation in SLC11A3 is associated with autosomal dominant hemochromatosis
2. Role of hemochromatosis C 282Y and H63D mutations in HFE gene in development of type 2 diabetes and diabetic nephropathy
3. Body iron stores are associated with serum insulin and blood glucose concentrations: Population study in 1,013 eastern Finnish men
4. Genetic determinants of type 2 diabetes
5. Free radicals and diabetes