Open AccessChildhood-onset inflammatory bowel diseases associated with mutation of Wiskott-Aldrich syndrome protein gene
Author(s) -
Takashi Ohya,
Masakatsu Yanagimachi,
Kentaro Iwasawa,
Shuichiro Umetsu,
Tsuyoshi Sogo,
Ayano Inui,
Tomoo Fujisawa,
Shuichi Ito
Publication year - 2017
Publication title -
world journal of gastroenterology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.427
H-Index - 155
eISSN - 2219-2840
pISSN - 1007-9327
DOI - 10.3748/wjg.v23.i48.8544
Subject(s) - wiskott–aldrich syndrome , wiskott–aldrich syndrome protein , primary immunodeficiency , inflammatory bowel disease , immunology , immunodeficiency , medicine , chronic granulomatous disease , pathogenesis , mutation , ulcerative colitis , crohn's disease , disease , biology , gene , pathology , genetics , immune system , actin cytoskeleton , cytoskeleton , cell
To screen primary immunodeficiency, Wiskott-Aldrich syndrome (WAS), and chronic granulomatous disease (CGD) among children with inflammatory bowel disease (IBD).