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OP0020 Identification of Multiple Sjögren’s Syndrome Susceptibility Loci

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Data

2013-06

Autor

Lessard, C. J.
Li, H.
Ice, J. A.
Adrianto, I.
Jonsson, R.
Illei, G. G.
Rischmueller, M.
Nordmark, G.
Mariette, X.
Miceli-Richard, C.
Herlenius, M. Wahren
Witte, T.
Brennan, M.
Omdal, R.
Gaffney, P. M.
Lessard, J. A.
Rönnblom, L.
Ng, W.-F.
Rhodus, N.
Segal, B.
Scofield, R. H.
James, J. A.
Anaya, Juan-ManuelAutoridad Universidad de Rosario
Montgomery, C. G.
Harley, J. B.
Sivils, K. Moser
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URI

https://doi.org/10.1136/annrheumdis-2013-eular.225
https://repository.urosario.edu.co/handle/10336/26499

Abstract

Background Sjögren’s syndrome (SS) is a common, clinically heterogeneous autoimmune disease characterized by exocrine gland dysfunction that involves both innate and adaptive immune responses. A complex genetic architecture has been hypothesized; however, genetic studies to date have been limited to candidate gene approaches.

Keyword

Sjögren’s syndrome ; autoimmune disease ;

Link para a fonte

https://ard.bmj.com/content/72/Suppl_3/A54.3...

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