山东大学教师主页 Yaoqin Gong Whole-exome Sequencing Identifies a Variant in TMEM132E Causing Autosomal-Recessive Nonsyndromic Hearing Loss DFNB99. Home

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Whole-exome Sequencing Identifies a Variant in TMEM132E Causing Autosomal-Recessive Nonsyndromic Hearing Loss DFNB99.

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Institution:基础医学院

Title of Paper: Whole-exome Sequencing Identifies a Variant in TMEM132E Causing Autosomal-Recessive Nonsyndromic Hearing Loss DFNB99.

Journal:Hum Mutat

First Author:Yaoqin Gong

All the Authors:邵常顺,刘奇迹,李江夏,蒋百春

Document Code:lw-169865

Volume:36

Issue:1

Page Number:98

Translation or Not:No

Date of Publication:2015-01

Release Time:2019-04-14

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Professor
Supervisor of Doctorate Candidates
Supervisor of Master's Candidates

Gender : Female

Alma Mater : 山东大学

Education Level : With Certificate of Graduation for Study as Master's Candidates

Degree : 博士

Status : Employed

School/Department : 基础医学院

Date of Employment : 1985-10-01

Faculty/School : Cheeloo College of Medicine, School of Basic Medical Sciences, School of Basic Medical Sciences, School of Basic Medical Sciences

Business Address : 趵突泉校区电镜楼211

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