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Molecular genetic studies of familial Meniere’s disease 被引量:3

Molecular genetic studies of familial Meniere’s disease
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摘要 Dear Editor.Meniere's disease(MD,MIM 156000),a chronic clinical illness affecting the inner ear,presents as episodes of spontaneous vertigo,fluctuating sensorineural hearing loss,tinnitus,and aural fullness.Endolymphatic hydrops in the cochlear duct and vestibular organs is considered the underlying histopathologic characteristic of MD.Most MD cases are sporadic(sporadic Meniere's disease,SMD),and approximately 4%-20%of patients with MD have a familial history.
出处 《Science China(Life Sciences)》 SCIE CAS CSCD 2019年第11期1557-1560,共4页 中国科学(生命科学英文版)
基金 supported by grants from the National Key Basic Research Program of China (2014CB943001) the National Natural Science Foundation of China (81530032 & 81830028)
关键词 Meniere FAMILIAL ORGANS
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