山东大学教师主页白晓卉 Five Novel Mutations in LOXHD1 Gene Were Identified to Cause Autosomal Recessive Nonsyndromic Hearing Loss in Four Chinese Families (vol 2020, pg 9, 2020) 中文主页

Five Novel Mutations in LOXHD1 Gene Were Identified to Cause Autosomal Recessive Nonsyndromic Hearing Loss in Four Chinese Families (vol 2020, pg 9, 2020)

发布时间：2021-10-12 点击次数：

所属单位：山东省耳鼻喉医院

论文名称：Five Novel Mutations in LOXHD1 Gene Were Identified to Cause Autosomal Recessive Nonsyndromic Hearing Loss in Four Chinese Families (vol 2020, pg 9, 2020)

发表刊物：BioMed Research International

第一作者：白晓卉

论文编号：A6DD45E6442A45BABC72E1AFA8DB828F

卷号：2020

是否译文：否

发表时间：2020-09

发布时间：2021-10-12

首页

科学研究

教学研究

获奖信息

招生信息

学生信息

我的相册

教师博客

更多

个人信息 Personal information

论文成果

Five Novel Mutations in LOXHD1 Gene Were Identified to Cause Autosomal Recessive Nonsyndromic Hearing Loss in Four Chinese Families (vol 2020, pg 9, 2020)