TY  - GEN
AU  - Tsuchida,Naomi
AU  - Kirino,Yohei
AU  - Soejima,Yutaro
AU  - Onodera,Masafumi
AU  - Arai,Katsuhiro
AU  - Tamura,Eiichiro
AU  - Ishikawa,Takashi
AU  - Kawai,Toshinao
AU  - Uchiyama,Toru
AU  - Nomura,Shigeru
AU  - Kobayashi,Daisuke
AU  - Taguri,Masataka
AU  - Mitsuhashi,Satomi
AU  - Mizuguchi,Takeshi
AU  - Takata,Atsushi
AU  - Miyake,Noriko
AU  - Nakajima,Hideaki
AU  - Miyatake,Satoko
AU  - Matsumoto,Naomichi
TI  - Haploinsufficiency of A20 caused by a novel nonsense variant or entire deletion of TNFAIP3 is clinically distinct from Behçet's disease
SN  - 1478-6362
PY  - 2020///0529
KW  - Adult
KW  - Behcet Syndrome
KW  - diagnosis
KW  - Child
KW  - DNA
KW  - genetics
KW  - DNA Mutational Analysis
KW  - Female
KW  - Genetic Predisposition to Disease
KW  - Genetic Testing
KW  - methods
KW  - Haploinsufficiency
KW  - Humans
KW  - Male
KW  - Mutation
KW  - Pedigree
KW  - Phenotype
KW  - Tumor Necrosis Factor alpha-Induced Protein 3
KW  - Tumor Necrosis Factor-alpha
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1186/s13075-019-1928-5
ER  -