Using a genetic isolate to identify novel genes causing otosclerosis, the most common cause of progressive hearing loss in Caucasians worldwide.
Using a genetic isolate to identify novel genes causing otosclerosis, the most common cause of progressive hearing loss in Caucasians worldwide.
批准号:
207296
负责人:
Abdelfatah Nelly F
金额:
$3.28万
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
项目状态:
已结题
起止时间:
2010-02-01 至 2012-02-01
中文摘要
耳硬化症是一种传导性听力损失,影响20多岁至30多岁的成年人,可能导致所有频率的严重听力损失。它是由中耳骨骼异常过度生长引起的小锤骨(距骨)过长。
英文摘要
Otosclerosis is a type of conductive hearing loss that affects adults in their 20s-30s and may lead to profound hearing loss across all frequencies. It is caused by abnormal overgrowth of bone in the middle ear that causes the small hammer bone (stapes) t
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
海外基金