Identification of causative variants in patients with non-syndromic hearing loss in the Minnan region, China by targeted next-generation sequencing | |
Han, Peng; Wu, Xiaohui; Gao, Xingqiang; Zhou, Yulin | |
刊名 | ACTA OTO-LARYNGOLOGICA
![]() |
2019 | |
卷号 | 139期号:3 |
关键词 | Non-syndromic hearing loss targeted next-generation sequencing GJB2 MT-RNR1 genetic diagnosis |
ISSN号 | 0001-6489 |
URL标识 | 查看原文 |
语种 | 英语 |
内容类型 | 期刊论文 |
URI标识 | http://www.corc.org.cn/handle/1471x/3600169 |
专题 | 复旦大学上海医学院 |
推荐引用方式 GB/T 7714 | Han, Peng,Wu, Xiaohui,Gao, Xingqiang,et al. Identification of causative variants in patients with non-syndromic hearing loss in the Minnan region, China by targeted next-generation sequencing[J]. ACTA OTO-LARYNGOLOGICA,2019,139(3). |
APA | Han, Peng,Wu, Xiaohui,Gao, Xingqiang,&Zhou, Yulin.(2019).Identification of causative variants in patients with non-syndromic hearing loss in the Minnan region, China by targeted next-generation sequencing.ACTA OTO-LARYNGOLOGICA,139(3). |
MLA | Han, Peng,et al."Identification of causative variants in patients with non-syndromic hearing loss in the Minnan region, China by targeted next-generation sequencing".ACTA OTO-LARYNGOLOGICA 139.3(2019). |
个性服务 |
查看访问统计 |
相关权益政策 |
暂无数据 |
收藏/分享 |
除非特别说明,本系统中所有内容都受版权保护,并保留所有权利。
修改评论