Haploinsufficiency of A20 caused by a novel nonsense variant or entire deletion of TNFAIP3 is clinically distinct from Behçet's disease.
about
Haploinsufficiency of A20 caused by a novel nonsense variant or entire deletion of TNFAIP3 is clinically distinct from Behçet's disease.
description
scientific article
@en
wetenschappelijk artikel
@nl
наукова стаття, опублікована в червні 2019
@uk
name
Haploinsufficiency of A20 caus ...... istinct from Behçet's disease.
@en
Haploinsufficiency of A20 caus ...... istinct from Behçet's disease.
@nl
type
label
Haploinsufficiency of A20 caus ...... istinct from Behçet's disease.
@en
Haploinsufficiency of A20 caus ...... istinct from Behçet's disease.
@nl
prefLabel
Haploinsufficiency of A20 caus ...... istinct from Behçet's disease.
@en
Haploinsufficiency of A20 caus ...... istinct from Behçet's disease.
@nl
P2093
P1476
Haploinsufficiency of A20 caus ...... distinct from Behçet's disease
@en
P2093
Daisuke Kobayashi
Eiichiro Tamura
Hideaki Nakajima
Katsuhiro Arai
Masafumi Onodera
Masataka Taguri
Naomi Tsuchida
Naomichi Matsumoto
Noriko Miyake
Satoko Miyatake
P356
10.1186/S13075-019-1928-5
P577
2019-06-04T00:00:00Z