The CTLA4 +49 A/G dimorphism is not associated with type 1 diabetes in Czech children-Reference-Cited by-同舟云学术

The CTLA4 +49 A/G dimorphism is not associated with type 1 diabetes in Czech children

Published:2002-05-30 Issue:3 Volume:29 Page:219-222
ISSN:0960-7420
Container-title:European Journal of Immunogenetics
language:en
Short-container-title:

Author:

Cinek O.,Dřevínek P.,Šumník Z.,Bendlová B.,Koloušková S.,Šnajderová M.,Vavřinec J.

Publisher

Wiley

Subject

Genetics,Immunology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1046/j.1365-2370.2002.00292.x/fullpdf

Reference13 articles.

1. CTLA4 alanine-17 confers genetic susceptibility to Graves’ disease and to type 1 diabetes mellitus;Donner;Journal of Clinical Endocrinology and Metabolism,1997

2. CTLA4 gene haplotypes cannot protect from IDDM in the presence of high-risk HLA DQ8 or DQ2 alleles in German families;Donner;Diabetes,1998

3. Genetic analysis of chromosome 2 in type 1 diabetes: analysis of putative loci IDDM7, IDDM12, and IDDM13 and candidate genes NRAMP1 and IA-2 and the interleukin-1 gene cluster;Esposito;IMDIAB Group. Diabetes,1998

4. CTLA-4 gene polymorphism is associated with predisposition to IDDM in a population from central Poland;Krokowski;Diabetes Metabolism,1998

5. IDDM12 (CTLA4) on 2q33 and IDDM13 on 2q34 in genetic susceptibility to type 1 diabetes (insulin-dependent);Larsen;Autoimmunity,1999

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