Targeted genomic capture and massively parallel sequencing of a Chinese family with non-syndromic low-frequency sensorineural hearing loss

摘要：

　　Background Wolfram syndrome gene 1 (WFS1) accounts for most of the familial non-syndromic low-frequency sensorineural hearing loss (LFSNHL) which is characterized by an unusual type of hearing loss in which frequencies <2000 Hz predominantly are affected.

作者: Yan Tizhen Tang Xiangrong Zeng Dingyuan Li Wugao Li Zhetao Luo Shiqiang Yang Yan Li Jingwen Wang Lin Cai Ren Tang Ning

作者单位: Key Laboratory of birth defects prevention and control, Liuzhou, Guangxi 545001, P.R.China;Departmen Center of Hearing, Liuzhou Municipal Maternity and Child Healthcare Hospital, Liuzhou, Guangxi 54500 Key Laboratory of birth defects prevention and control, Liuzhou, Guangxi 545001, P.R.China

会议类型: 国内会议

会议名称: 第十五次中国中西医结合耳鼻咽喉科专业委员会年会

会议地点: 浙江宁波

会议语种:英文

页码: 239-240

在线出版日期: 2016-07-29（万方平台首次上网日期，不代表论文的发表时间）