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Early-onset autoimmune disease due to a heterozygous loss-of-function mutation in TNFAIP3 (A20)
Christopher J A Duncan1, Emma Dinnigan1, Rachel Theobald1
1Primary Immunodeficiency Group, Institute for Cellular Medicine, Newcastle University, UK.
Annals of the Rheumatic Diseases
|June 30, 2017
Abstract
No abstract available in PubMed .
Keywords:
A20 haploinsufficiencyComplex autoimmunityImmune homeostasisMonogenic autoimmunityNF-κB regulationPrimary immunodeficiencyTNF signallingMore Related Videos
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