A dominantly-inherited Behcet-like disorder caused by haploinsufficiency of the TNFAIP3/A20 protein
2015 · Pediatric Rheumatology · 5 citations
https://doi.org/10.1186/1546-0096-13-s1-o71
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J Chae is an academic researcher from National Human Genome Research Institute. The author has contributed to research in topics: Inflammasome and immune disorders & Adenosine and Purinergic Signaling & Ocular Diseases and Behçet’s Syndrome. The author has an h-index of 1, co-authored 2 publications.
https://doi.org/10.1186/1546-0096-13-s1-o71
https://doi.org/10.1186/1546-0096-11-s1-a263
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