Haploinsufficiency of A20 caused by a novel nonsense variant or entire deletion of TNFAIP3 is clinically distinct from Behçet’s disease
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1478-6362
- Extent
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Online-Ressource
- Language
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Englisch
- Notes
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online resource.
- Bibliographic citation
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Haploinsufficiency of A20 caused by a novel nonsense variant or entire deletion of TNFAIP3 is clinically distinct from Behçet’s disease ; volume:21 ; number:1 ; day:4 ; month:6 ; year:2019 ; pages:1-12 ; date:12.2019
Arthritis Research & Therapy ; 21, Heft 1 (4.6.2019), 1-12, 12.2019
- Creator
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Tsuchida, Naomi
Kirino, Yohei
Soejima, Yutaro
Onodera, Masafumi
Arai, Katsuhiro
Tamura, Eiichiro
Ishikawa, Takashi
Kawai, Toshinao
Uchiyama, Toru
Nomura, Shigeru
Kobayashi, Daisuke
Taguri, Masataka
Mitsuhashi, Satomi
Mizuguchi, Takeshi
Takata, Atsushi
Miyake, Noriko
Nakajima, Hideaki
Miyatake, Satoko
Matsumoto, Naomichi
- Contributor
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SpringerLink (Online service)
- DOI
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10.1186/s13075-019-1928-5
- URN
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urn:nbn:de:101:1-2019092405462128542947
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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15.08.2025, 7:33 AM CEST
Data provider
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Associated
- Tsuchida, Naomi
- Kirino, Yohei
- Soejima, Yutaro
- Onodera, Masafumi
- Arai, Katsuhiro
- Tamura, Eiichiro
- Ishikawa, Takashi
- Kawai, Toshinao
- Uchiyama, Toru
- Nomura, Shigeru
- Kobayashi, Daisuke
- Taguri, Masataka
- Mitsuhashi, Satomi
- Mizuguchi, Takeshi
- Takata, Atsushi
- Miyake, Noriko
- Nakajima, Hideaki
- Miyatake, Satoko
- Matsumoto, Naomichi
- SpringerLink (Online service)
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