首页> 外文期刊>International journal of pediatric otorhinolaryngology >Mutation analysis of common GJB2, SCL26A4 and 12S rRNA genes among 380 deafness patients in northern China
【24h】

Mutation analysis of common GJB2, SCL26A4 and 12S rRNA genes among 380 deafness patients in northern China

机译:北方380例耳聋患者常见GJB2,SCL26A4和12S rRNA基因的突变分析

获取原文
获取原文并翻译 | 示例
       

摘要

Objectives: The molecular etiology of nonsyndromic deafness in Chinese population has not been investigated systematically, our study is aim to investigate the molecular etiology of nonsyndromic deafness patients from Northern China (Heilongjiang province), in order to provide genetic test and counseling to families.
机译:目的:我们的研究尚未在系统中尚未调查中国人口不健康耳聋的分子病因,旨在探讨中国北方(黑龙江省)的不健康耳聋患者的分子病因,以便为家庭提供遗传测试和咨询。

著录项

  • 来源
  • 作者单位

    Harbin Med Univ Affiliated Hosp 4 Dept Lab 37 Yiyuan St Harbin 150001 Heilongjiang Pr Peoples;

    Harbin Med Univ Affiliated Hosp 4 Dept Otolaryngol Head &

    Neck Surg 37 Yiyuan St Harbin 150001;

    Prov Hosp Heilongjiang Dept Angiosis 82 Zhongshan Rd Harbin 150001 Heilongjiang Pr Peoples R;

    Harbin Med Univ Affiliated Hosp 4 Dept Otolaryngol Head &

    Neck Surg 37 Yiyuan St Harbin 150001;

    Harbin Med Univ Affiliated Hosp 4 Dept Otolaryngol Head &

    Neck Surg 37 Yiyuan St Harbin 150001;

    Harbin Med Univ Affiliated Hosp 4 Dept Otolaryngol Head &

    Neck Surg 37 Yiyuan St Harbin 150001;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 耳鼻咽喉科学;
  • 关键词

    Nonsyndromic deafness; GJB2; SLC26A4; 12S rRNA;

    机译:非合成症耳聋;GJB2;SLC26A4;12S rRNA;

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号