关键词: TNFAIP3 autoimmune disorder autosomal-dominant-inherited disease expressivity gene mutation haploinsufficiency of A20 intestinal Behçet's disease whole exome sequencing
Mesh : Adult Asians / genetics Behcet Syndrome / genetics Female Genetic Predisposition to Disease / genetics Haploinsufficiency / genetics Humans Male Pedigree Tumor Necrosis Factor alpha-Induced Protein 3 / genetics
来 源:
DOI:10.3389/fimmu.2020.01414
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