Haploinsufficiency of TNFAIP3 (A20) by germline mutation is involved in autoimmune lymphoproliferative syndrome

Autoimmune diseases in children are rare and can be difficult to diagnose. Autoimmune lymphoproliferative syndrome (ALPS) is a well-characterized pediatric autoimmune disease caused by mutations in genes associated with the FAS-dependent apoptosis pathway. In addition, various genetic alterations ar...

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Published inJournal of allergy and clinical immunology Vol. 139; no. 6; pp. 1914 - 1922
Main Authors Takagi, Masatoshi, Ogata, Shohei, Ueno, Hiroo, Yoshida, Kenichi, Yeh, Tzuwen, Hoshino, Akihiro, Piao, Jinhua, Yamashita, Motoy, Nanya, Mai, Okano, Tsubasa, Kajiwara, Michiko, Kanegane, Hirokazu, Muramatsu, Hideki, Okuno, Yusuke, Shiraishi, Yuichi, Chiba, Kenichi, Tanaka, Hiroko, Bando, Yuki, Kato, Motohiro, Hayashi, Yasuhide, Miyano, Satoru, Imai, Kohsuke, Ogawa, Seishi, Kojima, Seiji, Morio, Tomohiro
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 01.06.2017
Elsevier Limited
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