TNFa microsatellite polymorphism modulates the risk of IDDM in caucasians with the high-risk genotype HLA DQA1*0501-DQB1*0201/DQA1*0301- DQB1*0302

Diabetes

Volumn 46, Issue 9, 1997, Pages 1514-1515

  Moghaddam, Payman Hanifi ^a   Zwinderman, Aeilko H ^b   De Knijff, Peter ^b   Roep, Bart O ^a   Schipper, Ron F ^a   Van Der Auwera, Bart ^c   Naipal, Albert ^a   Gorus, Frans ^d   Schuit, Frans ^c   Giphart, Marins J ^a  

^a LEIDEN UNIVERSITY MEDICAL CENTER   (Netherlands)

^b LEIDEN UNIVERSITY   (Netherlands)

^c FREE UNIVERSITY OF BRUSSELS   (Belgium)

^d VRIJE UNIVERSITEIT BRUSSEL   (Belgium)

Author keywords

[No Author keywords available]

Indexed keywords

CYTOKINE; HLA DQ ANTIGEN; TUMOR NECROSIS FACTOR ALPHA;

ARTICLE; AUTOIMMUNITY; CONTROLLED STUDY; DIABETES MELLITUS; GENETIC POLYMORPHISM; GENOTYPE; HIGH RISK PATIENT; HLA SYSTEM; HUMAN; INSULIN DEPENDENT DIABETES MELLITUS; MAJOR CLINICAL STUDY; PRIORITY JOURNAL; RISK ASSESSMENT;

EID: 0006747979     PISSN: 00121797     EISSN: None     Source Type: Journal    
DOI: 10.2337/diab.46.9.1514     Document Type: Article

References (9)

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3. Vandewalle CL, Decraene T, Schuit FC, De Leeuw IH, Pipeleers DG, Gorus FK, the Belgian Diabetes Registry: Insulin autoantibodies and high titre islet cell antibodies are preferentially associated with the HLA DQA1*0301-DQB1*0302 haplotype at clinical type 1 (insulin-dependent) diabetes mellitus before age 10 years, but not at onset between age 10 and 40 years: the Belgian Diabetes Registry. Diabetologia 36:1155-1162, 1993
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