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Childhood-onset inflammatory bowel diseases associated with mutation of Wiskott-Aldrich syndrome protein gene

AIM: To screen primary immunodeficiency, Wiskott-Aldrich syndrome (WAS), and chronic granulomatous disease (CGD) among children with inflammatory bowel disease (IBD). METHODS: This was a single-center retrospective study. Eighteen children with IBD were investigated. We analyzed their expression of...

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Bibliographische Detailangaben
Veröffentlicht in:World J Gastroenterol
Hauptverfasser: Ohya, Takashi, Yanagimachi, Masakatsu, Iwasawa, Kentaro, Umetsu, Shuichiro, Sogo, Tsuyoshi, Inui, Ayano, Fujisawa, Tomoo, Ito, Shuichi
Format: Artigo
Sprache:Inglês
Veröffentlicht: Baishideng Publishing Group Inc 2017
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Online Zugang:https://ncbi.nlm.nih.gov/pmc/articles/PMC5752714/
https://ncbi.nlm.nih.gov/pubmed/29358862
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3748/wjg.v23.i48.8544
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