絞り込み

16501

広告

A20 haploinsufficiency (HA20): clinical phenotypes and disease course of patients with a newly recognised NF-kB-mediated autoinflammatory disease.

著者 Aeschlimann FA , Batu ED , Canna SW , Go E , Gül A , Hoffmann P , Leavis HL , Ozen S , Schwartz DM , Stone DL , van Royen-Kerkof A , Kastner DL , Aksentijevich I , Laxer RM
Ann Rheum Dis.2018 Jan 09 ; ():.
この記事をPubMed上で見るPubMedで表示
この記事をGoogle翻訳上で見る Google翻訳で開く

スターを付ける スターを付ける     (17view , 0users)

Full Text Sources

The association between mutations in TNFAIP3, encoding the NF-kB regulatory protein A20, and a new autoinflammatory disease has recently been recognised. This study aims at describing the clinical phenotypes and disease course of patients with A20 haploinsufficiency (HA20).
PMID: 29317407 [PubMed - as supplied by publisher]
印刷用ページを開く Endnote用テキストダウンロード