OP0020 Identification of Multiple Sjögren’s Syndrome Susceptibility Loci

Data
2013-06Autor
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-Manuel
Montgomery, C. G.
Harley, J. B.
Sivils, K. Moser
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URI
https://doi.org/10.1136/annrheumdis-2013-eular.225https://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.
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