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Germline and somatic genetic variations of TNFAIP3 in lymphoma complicating primary Sjögren’s syndrome
Several autoimmune diseases, including primary Sjögren’s syndrome (pSS), are associated with an increased risk for lymphoma. Polymorphisms of TNFAIP3, which encodes the A20 protein that plays a key role in controlling nuclear factor κB activation, have been associated with several autoimmune disease...
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| Hauptverfasser: | , , , , , , , , , , , , , , , , , , |
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| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
American Society of Hematology
2013
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3862283/ https://ncbi.nlm.nih.gov/pubmed/24159176 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1182/blood-2013-05-503383 |
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