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The Journal of Clinical Endocrinology and Metabolism|October 13, 2009
Homozygosity of the polymorphism MICA5.1 identifies extreme risk of progression to overt adrenal insufficiency among 21-hydroxylase antibody-positive patients with type 1 diabetesTaylor M Triolo, Erin E Baschal, Taylor K Armstrong, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 13, 2006
Extreme genetic risk for type 1A diabetesTheresa A Aly, Akane Ide, Mohamed M Jahromi, et al.
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