一个遗传性聋伴前庭功能障碍家系的表型研究与相关基因探讨
A Study of Audiological Characteristics and Gene Mutations in a Family with Hereditary Hearing Impairment and Vestibular Dysfunction
刘玉和;马祎楠;柯肖枚;钟贞;戚豫;肖水芳;
1:北京大学第一医院耳鼻咽喉头颈外科
2:北京大学第一医院中心实验室
摘要关键词基金项目(Foundation):作者参考文献1Robertson NG,Lu L,Heller S,et al.Mutationin a novel co-chlear gene cause DFNA9,a human nonsyndromic deafness with vestibular dysfunction[J].Nature Genet,1998,20:299.
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