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
• 起止时间: 2010-10-01 至 2011-10-01
• 项目状态: 已结题
• 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

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

儿童遗传性疾病虽然个别罕见，但总体上很常见，影响着加拿大约 500,000 名儿童的生活。这些疾病会导致各种医疗问题，包括出生缺陷、智力障碍、困难等。