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Finding of Rare Disease Genes in Canada (FORGE CANADA)

Finding of Rare Disease Genes in Canada (FORGE CANADA)
加拿大罕见病基因发现（FORGE CANADA）
批准号：
222201
负责人：
Boycott Kym M
金额：
$89.24万
依托单位：
Children's Hospital of Eastern Ontario Research Institute Inc
依托单位国家：
加拿大
项目类别：
Operating Grants
财政年份：
2010
资助国家：
加拿大
项目状态：
已结题
起止时间：
2010-10-01 至 2011-10-01
来源：
https://webapps.cihr-irsc.gc.ca/decisions/p/project_details.html?applId=222201&lang=en
关键词：
Gene Identification Mendelian Disorders Rare Disease

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中文摘要
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英文摘要
Genetic disorders of children are individually rare but collectively frequent, affecting the lives of approximately 500,000 children in Canada. These disorders cause a variety of medical problems including birth defects, intellectual disability, difficult
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A Canadian knowledge-to-action roadmap for evidence-informed implementation of first-tier clinical genome-wide sequencing for rare disease (K2A-RD)
Care4Rare-SOLVE
Canada Research Chair - Tier 1
  • 批准号：
    404325
  • 项目类别：
  • 资助金额：
    $101.99万
  • 财政年份：
    2018
  • 负责人：
    Boycott Kym M
  • 依托单位：
    University of Ottawa
Care4Rare Canada: Harnessing multi-omics to deliver innovative diagnostic care for rare genetic diseases in Canada (C4R-SOLVE)
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