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Skinningsrud B, Husebye ES, Pearce SH, et al. 
Polymorphisms in CLEC16A and CIITA at 16p13 are associated with primary adrenal insufficiency. [JOURNAL ARTICLE]
J Clin Endocrinol Metab 2008 Jul 1.
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Jennings CE, Owen CJ, Wilson V, et al. 
A haplotype of the CYP27B1 promoter is associated with autoimmune Addison's disease but not with Graves' disease in a UK population. [Journal Article]
J Mol Endocrinol 2005 Jun; 34(3):859-63.
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Kemp EH, Ajjan RA, Husebye ES, et al. 
A cytotoxic T lymphocyte antigen-4 (CTLA-4) gene polymorphism is associated with autoimmune Addison's disease in English patients. [Journal Article]
Clin Endocrinol (Oxf) 1998 Nov; 49(5):609-13.
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Blomhoff A, Lie BA, Myhre AG, et al. 
Polymorphisms in the cytotoxic T lymphocyte antigen-4 gene region confer susceptibility to Addison's disease. [Journal Article]
J Clin Endocrinol Metab 2004 Jul; 89(7):3474-6.
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Wolff AS, Myhr KM, Vedeler CA, et al. 
Fcgamma Receptor Polymorphisms are not Associated with Autoimmune Addison's Disease. [Journal Article]
Scand J Immunol 2007 Jun; 65(6):555-8.
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Maclaren NK, Riley WJ 
Inherited susceptibility to autoimmune Addison's disease is linked to human leukocyte antigens-DR3 and/or DR4, except when associated with type I autoimmune polyglandular syndrome. [Journal Article]
J Clin Endocrinol Metab 1986 Mar; 62(3):455-9.
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Ghaderi M, Gambelunghe G, Tortoioli C, et al. 
MHC2TA single nucleotide polymorphism and genetic risk for autoimmune adrenal insufficiency. [JOURNAL ARTICLE]
J Clin Endocrinol Metab 2006 Jul 18.
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Owen CJ, Kelly H, Eden JA, et al. 
ANALYSIS OF THE FC-RECEPTOR LIKE-3 (FCRL3) LOCUS IN CAUCASIANS WITH AUTOIMMUNE DISORDERS SUGGESTS A COMPLEX PATTERN OF DISEASE ASSOCIATION. [JOURNAL ARTICLE]
J Clin Endocrinol Metab 2007 Jan 2.
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Myhre R, Klungland H, Farrer MJ, et al. 
Genetic association study of synphilin-1 in idiopathic Parkinson's disease. [JOURNAL ARTICLE]
BMC Med Genet 2008 Mar 21; 9(1):19.
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