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Molecular Analysis Of Human Hereditary Deafness

Molecular Analysis Of Human Hereditary Deafness
人类遗传性耳聋的分子分析
批准号：
6531866
负责人：
Andrew J Griffith
金额：
$0.0万
依托单位：
NATIONAL INSTITUTE ON DEAFNESS AND OTHER COMMUNICATION DISORDERS
依托单位国家：
美国
项目类别：
财政年份：
--
资助国家：
美国
项目状态：
未结题
起止时间：
至
来源：
https://reporter.nih.gov/project-details/6531866
关键词：
Asians adolescence (12-20) child (0-11) clinical research congenital deafness gene mutation genetic disorder human subject molecular genetics nervous system disorder epidemiology neurogenetics

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中文摘要
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英文摘要
We have identified a novel family of genes in which mutations can cause hereditary hearing loss in humans. We have characterized the genetic epidemiology of deafness caused by mutations in the Pendred syndrome in far east Asian individuals.
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