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首页> 外文期刊>The American journal of otology >Cracking the auditory genetic code: part II. Syndromic hereditary hearing impairment.
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Cracking the auditory genetic code: part II. Syndromic hereditary hearing impairment.

机译：破解听觉遗传密码：第二部分。症状性遗传性听力障碍。

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OBJECTIVE: The application of molecular genetic techniques to the study of hereditary hearing impairment has contributed significantly to our understanding of auditory physiology and disease processes. This article reviews the current state of our knowledge regarding the genes associated with syndromic hereditary hearing impairment. DATA SOURCES: Data were obtained from the Medline database and the internet. STUDY SELECTION: Articles relevant to genetics of syndromic deafness were selected. DATA EXTRACTION: Data pertaining to phenotypes, location of genes, identification of genes, and implications for hearing were extracted. CONCLUSION: Significant progress has been made in understanding the molecular pathogenesis of deafness.
机译：目的：分子遗传学技术在遗传性听力障碍研究中的应用为我们对听觉生理和疾病过程的理解做出了重要贡献。本文回顾了有关与遗传性遗传性听力障碍相关的基因的知识的现状。数据来源：数据来自Medline数据库和互联网。研究选择：选择与综合征性耳聋遗传相关的文章。数据提取：提取与表型，基因位置，基因鉴定和听觉有关的数据。结论：在耳聋的分子发病机理研究中取得了重要进展。

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