Common genetic variation in the autoimmune regulator (AIRE) locus is associated with autoimmune Addison’s disease in Sweden
Author:
Publisher
Springer Science and Business Media LLC
Subject
Multidisciplinary
Link
http://www.nature.com/articles/s41598-018-26842-2.pdf
Reference81 articles.
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2. Mitchell, A. L. & Pearce, S. H. Autoimmune Addison disease: pathophysiology and genetic complexity. Nat Rev Endocrinol 8, 306–316, https://doi.org/10.1038/nrendo.2011.245 (2012).
3. Hsieh, S. & White, P. C. Presentation of primary adrenal insufficiency in childhood. J Clin Endocrinol Metab 96, E925–928, https://doi.org/10.1210/jc.2011-0015 (2011).
4. Winqvist, O., Karlsson, F. A. & Kämpe, O. 21-Hydroxylase, a major autoantigen in idiopathic Addison’s disease. Lancet 339, 1559–1562 (1992).
5. Falorni, A. et al. Determination of 21-hydroxylase autoantibodies: inter-laboratory concordance in the Euradrenal International Serum Exchange Program. Clinical Chemistry and Laboratory Medicine. 53, 1761–1770, https://doi.org/10.1515/cclm-2014-1106 (2015).
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