Defining the molecular mechanism in hereditary cytoplasmic body myopathy with early respiratory failure: implications for understanding ventilatory failure in muscular dystrophies

定义遗传性细胞质体肌病伴早期呼吸衰竭的分子机制：对理解肌营养不良症通气衰竭的意义

• 批准号: 208695
• 负责人: Pfeffer Gerald
• 金额: $ 1.46万
• 依托单位: University of Newcastle upon Tyne (UK)
• 依托单位国家: 加拿大
• 项目类别: Fellowship Programs
• 财政年份: 2010
• 资助国家: 加拿大
• 起止时间: 2010-02-01 至 2014-02-01
• 项目状态: 已结题
• 来源: https://webapps.cihr-irsc.gc.ca/decisions/p/project_details.html?applId=208695&lang=en
• 关键词: Genetics; Hereditary Cytoplasmic Body Myopathy; Muscular Dystrophy; Neuromuscular Disease; Respiratory Failure

Hereditary cytoplasmic body myopathy with early respiratory failure (HCBM) is a hereditary muscle disease which selectively affects muscles required for breathing, early in its disease course (among other select muscles). Respiratory dysfunction also occu

遗传性胞浆体肌病伴早期呼吸衰竭（HCBM）是一种遗传性肌肉疾病，在其病程早期选择性地影响呼吸所需的肌肉（以及其他选择的肌肉）。呼吸功能障碍也会发生。