Analysis of non-coding regions and novel gene discovery: Exploring the unknown in inherited neuromuscular disorders.

非编码区分析和新基因发现：探索遗传性神经肌肉疾病的未知因素。

• 批准号: 473739
• 负责人: Polavarapu Kiran
• 金额: $ 9.83万
• 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: Fellowship Programs
• 财政年份: 2022
• 资助国家: 加拿大
• 起止时间: 2022-10-01 至 2025-10-01
• 项目状态: 未结题
• 来源: https://webapps.cihr-irsc.gc.ca/decisions/p/project_details.html?applId=473739&lang=en
• 关键词: Diagnostics; Gene Discovery; Genetics; Neuromuscular Disease; Non-Coding Regions

Neuromuscular disorders are rare inherited diseases affecting both children and adults with muscle weakness as a common feature due to defects in the function of muscles and/or nerves. While more than 600 genes have been identified as causing neuromuscula

神经肌肉疾病是影响儿童和成人的罕见遗传性疾病，由于肌肉和/或神经功能缺陷，肌肉无力是一种常见特征。而超过600个基因已被确定为导致神经肌肉