Functional studies of a genetic mutation in the development of a Wiskott-Aldrich-like syndrome in paediatric patients
Functional studies of a genetic mutation in the development of a Wiskott-Aldrich-like syndrome in paediatric patients
儿童患者 Wiskott-Aldrich 样综合征发生过程中基因突变的功能研究
批准号：
363787
负责人：
Leung Gabriella
金额：
$3.28万
依托单位国家：
加拿大
项目类别：
Fellowship Programs
财政年份：
2016
资助国家：
加拿大
项目状态：
已结题
起止时间：
2016-11-01 至 2018-11-01
中文摘要
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英文摘要
Canada has one of the highest rates of inflammatory bowel disease (IBD) in the world with 1 in 150 affected, the incidence of which is also increasing globally. The pathogenesis of IBD is the combination of many factors including the microbiota, immune sy
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