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Haploinsufficiency of A20 caused by a novel nonsense variant or entire deletion of TNFAIP3 is clinically distinct from Behçet’s disease
Tsuchida, Naomi, Kirino, Yohei, Soejima, Yutaro, Onodera, Masafumi, Arai, Katsuhiro, Tamura, Eiichiro, Ishikawa, Takashi, Kawai, Toshinao, Uchiyama, Toru, Nomura, Shigeru, Kobayashi, Daisuke, Taguri,Volume:
21
Language:
english
Journal:
Arthritis Research & Therapy
DOI:
10.1186/s13075-019-1928-5
Date:
December, 2019
File:
PDF, 2.09 MB
english, 2019