Variants in PTPN22 and SMOC2 genes and the risk of thyroid disease in the Jordanian Arab population
Author:
Publisher
Springer Science and Business Media LLC
Subject
Endocrinology,Endocrinology, Diabetes and Metabolism
Link
http://link.springer.com/content/pdf/10.1007/s12020-013-9908-z.pdf
Reference35 articles.
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3. T.F. Davies, R. Latif, X. Yin, New genetic insights from autoimmune thyroid disease. J. Thyroid. Res. 2012, 623852 (2012)
4. L.Q. Gu, W. Zhu, S.X. Zhao, L. Zhao, M.J. Zhang, B. Cui, H.D. Song, G. Ning, Y.J. Zhao, Clinical associations of the genetic variants of CTLA-4, Tg, TSHR, PTPN22, PTPN12 and FCRL3 in patients with Graves’ disease. Clin. Endocrinol. (Oxf). 72, 248–255 (2010)
5. N. Eriksson, J.Y. Tung, A.K. Kiefer, D.A. Hinds, U. Francke, J.L. Mountain, C.B. Do, Novel associations for hypothyroidism include known autoimmune risk loci. PLoS ONE 7, e34442 (2012)
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