Tsuchida, Naomi <br/><br/>
Haploinsufficiency of A20 caused by a novel nonsense variant or entire deletion of TNFAIP3 is clinically distinct from Behçet's disease.  [electronic resource] 

 -  Arthritis research & therapy  06 2019 
 - 137 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1478-6362 
<br/><br/><label>Standard No.: </label>10.1186/s13075-019-1928-5  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Behcet Syndrome--diagnosis<br/>Child<br/>DNA--genetics<br/>DNA Mutational Analysis<br/>Female<br/>Genetic Predisposition to Disease<br/>Genetic Testing--methods<br/>Haploinsufficiency--genetics<br/>Humans<br/>Male<br/>Mutation<br/>Pedigree<br/>Phenotype<br/>Tumor Necrosis Factor alpha-Induced Protein 3--genetics<br/>Tumor Necrosis Factor-alpha