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Identification of Genes and Pathways for Rare Mendelian Neurological Disease

Identification of Genes and Pathways for Rare Mendelian Neurological Disease
罕见孟德尔神经系统疾病的基因和通路的鉴定
批准号：
209019
负责人：
Boycott Kym M
金额：
$20.4万
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：
Salary Programs
财政年份：
2010
资助国家：
加拿大
项目状态：
已结题
起止时间：
2010-07-01 至 2012-07-01
来源：
https://webapps.cihr-irsc.gc.ca/decisions/p/project_details.html?applId=209019&lang=en
关键词：
Gene Identification Mendelian Disease Neurodegeneration Neurodevelopment Neurogenetics

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中文摘要
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英文摘要
It has been 20 years since the official commencement of the Human Genome Project and six years since its completion and with the recent introduction of instruments capable of producing millions of DNA sequence reads in a single run there are now indicatio
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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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