Mutation analysis of common deafness genes among 1,201 patients with non-syndromic hearing loss in Shanxi Province.

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第一作者： Yongan,Zhou

第一单位： Shanxi Medical University Second Affiliated Hospital, Taiyuan, Shanxi, China.

作者： Yongan,Zhou ^[1] ; Chao,Li ^[2] ; Min,Li ^[2] ; Zhonghua,Zhao ^[3] ; Shuxiong,Tian ^[2] ; Hou,Xia ^[2] ; Peixian,Liu ^[1] ; Yaxin,Han ^[2] ; Ruirui,Ren ^[2] ; Jianping,Chen ^[2] ; Caihong,Jia ^[1] ; Wei,Guo ^[4]

作者单位： Shanxi Medical University Second Affiliated Hospital, Taiyuan, Shanxi, China. ^[1] The Graduate School, Shanxi Medical University, Taiyuan, Shanxi, China. ^[2] Institute of Biomedical Sciences, Shanxi University, Taiyuan, Shanxi, China. ^[3] Xinzhou Traditional Chinese Medicine Hospital, Xinzhou, Shanxi, China. ^[4]

关键词 GJB2 SLC26A4 mtDNA 12S rRNA gene non-syndromic hearing loss

主题词青少年(Adolescent);成年人(Adult);儿童(Child);儿童, 学龄前(Child, Preschool);中国(China);连接蛋白类(Connexins);聋(Deafness);女(雌)性(Female);人类(Humans);婴儿(Infant);男(雄)性(Male);RNA, 核糖体(RNA, Ribosomal)

DOI 10.1002/mgg3.537

PMID 30693673

发布时间 2021-12-04

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Molecular genetics & genomic medicine

2019年7卷3期

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Mutation analysis of common deafness genes among 1,201 patients with non-syndromic hearing loss in Shanxi Province.

Molecular genetics & genomic medicine

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Molecular genetics & genomic medicine

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Mutation analysis of common deafness genes among 1,201 patients with non-syndromic hearing loss in Shanxi Province.

Molecular genetics & genomic medicine

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Molecular genetics & genomic medicine

相关期刊

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