中华耳科学杂志2017，Vol.15Issue(5)：586-590,5.DOI:10.3969/j.issn.1672-2922.2017.017.
梅尼埃病的基因学研究新进展
Recent Advances in Genetics of Ménière's Disease
摘要
Abstract
Ménière's disease (MD) is an extremely complex inner ear disorder. The primary histopathological correlate is endolymphatic hydrops. Although its etiology is not known, familial clustering and genetic heterogeneity strongly suggest that genetic factors play a role in the development of MD. In this review, we will explore the numerous reports published in the literature and summarize recent advances in genetics of Ménière's disease.关键词
梅尼埃病/基因/研究进展Key words
Ménière's Disease/Gene/Research Progress分类
医药卫生引用本文复制引用
徐舒舒,袁进,赵洪春,王延飞..梅尼埃病的基因学研究新进展[J].中华耳科学杂志,2017,15(5):586-590,5.基金项目
滨州医学院科技计划(No:BY2011KJ007) （No:BY2011KJ007）
国家自然科学基金(No:81500797) This study was supported by the project of Binzhou Medical University Science and Technology Plan (No:BY2011KJ007) and project of National Natural Science Fund (No:81500797). （No:81500797）
