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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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Veröffentlicht in: | World J Gastroenterol |
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Hauptverfasser: | , , , , , , , |
Format: | Artigo |
Sprache: | Inglês |
Veröffentlicht: |
Baishideng Publishing Group Inc
2017
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Schlagworte: | |
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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