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Autoimmune polyendocrine syndrome type 1 and NALP5, a parathyroid autoantigen

Date Issued
2008-01-01
Author(s)
Alimohammadi, Mohammad
Björklund, Peyman
Hallgren, Asa
Pöntynen, Nora
Szinnai, Gabor  
Shikama, Noriko
Keller, Marcel P
Ekwall, Olov
Kinkel, Sarah A
Husebye, Eystein S
Gustafsson, Jan
Rorsman, Fredrik
Peltonen, Leena
Betterle, Corrado
Perheentupa, Jaakko
Akerström, Göran
Westin, Gunnar
Scott, Hamish S
Holländer, Georg A  
Kämpe, Olle
DOI
10.1056/nejmoa0706487
Abstract
Autoimmune polyendocrine syndrome type 1 (APS-1) is a multiorgan autoimmune disorder caused by mutations in AIRE, the autoimmune regulator gene. Though recent studies concerning AIRE deficiency have begun to elucidate the molecular pathogenesis of organ-specific autoimmunity in patients with APS-1, the autoantigen responsible for hypoparathyroidism, a hallmark of APS-1 and its most common autoimmune endocrinopathy, has not yet been identified.
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