Mutations in HFE, the hemochromatosis candidate gene, in patients with NIDDM [7]

Diabetes Care

Volumn 21, Issue 8, 1998, Pages 1371-1372

  Dubois Laforgue, D ^a   Caillat Zucman, S ^a   Djilali Saiah, I ^a   Larger, E ^a   Mercadier, A ^a   Boitard, C ^a   Bach, J F ^a   Timsit, J ^a  

^a HÔPITAL NECKER ENFANTS MALADES   (France)

Author keywords

[No Author keywords available]

Indexed keywords

COMORBIDITY; DISEASE ASSOCIATION; FERRITIN BLOOD LEVEL; GENE MUTATION; GENETIC DISORDER; GLUCOSE BLOOD LEVEL; HEMOCHROMATOSIS; HUMAN; IRON BLOOD LEVEL; LETTER; NON INSULIN DEPENDENT DIABETES MELLITUS; PREVALENCE;

AMINO ACID SUBSTITUTION; ASPARTIC ACID; CYSTEINE; DIABETES MELLITUS, TYPE 2; HEMOCHROMATOSIS; HISTIDINE; HISTOCOMPATIBILITY ANTIGENS CLASS I; HLA ANTIGENS; HOMOZYGOTE; HUMANS; MAJOR HISTOCOMPATIBILITY COMPLEX; MEMBRANE PROTEINS; POINT MUTATION; REFERENCE VALUES; TYROSINE;

EID: 0031880544     PISSN: 01495992     EISSN: None     Source Type: Journal    
DOI: 10.2337/diacare.21.8.1371     Document Type: Letter

References (9)