Lack of association of the vitamin D receptor gene with Graves' disease in UK Caucasians
Author:
Publisher
Wiley
Subject
Endocrinology, Diabetes and Metabolism,Endocrinology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2265.2004.02015.x/fullpdf
Reference44 articles.
1. MHC class II region, CTLA4 gene, and ophthalmopathy in patients with Graves' disease
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3. Susceptibility and resistance alleles of human leukocyte antigen (HLA) DQA1 and HLA DQB1 are shared in endocrine autoimmune disease
4. Cloning and expression of full-length cDNA encoding human vitamin D receptor.
5. Signatures of natural selection in the human genome
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