Identifying novel genes causing otosclerosis, the most common cause of progressive hearing loss in Caucasians worldwide, using Newfoundland's founder population.
Identifying novel genes causing otosclerosis, the most common cause of progressive hearing loss in Caucasians worldwide, using Newfoundland's founder population.
利用纽芬兰的创始人人群识别导致耳硬化症的新基因，耳硬化症是全世界白种人进行性听力损失的最常见原因。
批准号：
207295
负责人：
Young Terry-Lynn
金额：
$18.25万
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
项目状态：
已结题
起止时间：
2010-03-01 至 2013-03-01
中文摘要
翻译
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，并可能进展为严重的听力损失。这是由于中耳中的微小骨骼异常过度生长，导致这些正常活动的骨骼被冻结所致。在……里面
英文摘要
Otosclerosis is a type of conductive hearing loss that affects adults in their 20s-30s and may progress to profound hearing loss. It is caused by abnormal overgrowth of the tiny bones in the middle ear, causing these normally mobile bones to "freeze". In
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会议论文
The Genomics and Proteomics of TMEM43, its association with Arrythmogenic Right Ventricular Cardiomyopathy and the translation of this knowledge to improve the health care of those affected.
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批准号：174406
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项目类别：Operating Grants
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资助金额：$0.0万
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财政年份：2008
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负责人：Young Terry-Lynn
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依托单位：
海外基金
