Inherited Disorders of Vitamin B12 Metabolism

维生素 B12 代谢遗传性疾病

• 批准号: 172017
• 负责人: Gravel Roy A
• 金额: $ 84万
• 依托单位: University of Calgary
• 依托单位国家: 加拿大
• 项目类别: Operating Grants
• 财政年份: 2008
• 资助国家: 加拿大
• 起止时间: 2008-09-01 至 2013-09-01
• 项目状态: 已结题
• 来源: https://webapps.cihr-irsc.gc.ca/decisions/p/project_details.html?applId=172017&lang=en
• 关键词: Caenorhabditis Elegans; Complementation Groups; Mitochondria; Mutation; Protein Complex; Vitamin B12

Vitamin B12 is an essential nutrient by helping maintain the metabolic activity of all cells. At least eight genetic diseases have been discovered which are blocked in the metabolism of vitamin B12 to its active forms, resulting in severe, potentially fat

维生素B12是一种必需的营养素，有助于维持所有细胞的代谢活动。至少有八种遗传疾病已经被发现，它们阻碍了维生素B12向活性形式的代谢，导致严重的、潜在的肥胖