New SNP variants of MARVELD2 (DFNB49) associated with non-syndromic hearing loss in Chinese population 中国人群中非综合征耳聋相关 MARVELD2 (DFNB49)基因新单核苷酸多态性位点分析

doi:10.1631/jzus.B1700185

科研成果详情

名称	New SNP variants of MARVELD2 (DFNB49) associated with non-syndromic hearing loss in Chinese population 中国人群中非综合征耳聋相关 MARVELD2 (DFNB49)基因新单核苷酸多态性位点分析
作者	Zheng, Jing 1,2; Meng, Wen-fang 1,2; Zhang, Chao-fan 2; Liu, Han-qing 2; Yao, Juan 3; Wang, Hui 3; Chen, Ye 1,2; Guan, Min-xin 1,2
发表期刊	Journal of Zhejiang University: Science B;
语种	中文
原始文献类型	Letter
其他关键词	TRICELLULIN ; PROTEIN ; IMPAIRMENT ; PAKISTANI ; MUTATIONS ; JUNCTIONS ; GENETICS
资助项目	National Basic Research Priorities Program of China[2014CB541702,2014CB541704];National Natural Science Foundation of China[81470685,81600817];Zhejiang Provincial Public Welfare Technology Applied Research Project[2016C33148];
出版者	ZHEJIANG UNIV
ISSN	1673-1581
EISSN	1862-1783
卷号	20
期号	2
页码	164-169
DOI	10.1631/jzus.B1700185
页数	6
WOS类目	Biochemistry & Molecular Biology ; Biotechnology & Applied Microbiology ; Medicine, Research & Experimental
WOS研究方向	Biochemistry & Molecular Biology ; Biotechnology & Applied Microbiology ; Research & Experimental Medicine
WOS记录号	WOS:000457593400007
收录类别	SCOPUS ; SCIE
发布日期	2019-02-01
URL	查看原文
PubMed ID	30406641
通讯作者地址	[Chen, Ye]Zhejiang Univ, Childrens Hosp, Div Med Genet & Genom, Sch Med, Hangzhou 310003, Zhejiang, Peoples R China. ; [Chen, Ye]Zhejiang Univ, Inst Genet, Hangzhou 310058, Zhejiang, Peoples R China.
Scopus学科分类	Biochemistry, Genetics and Molecular Biology (all);Veterinary (all);Pharmacology, Toxicology and Pharmaceutics (all)
SCOPUSEID	2-s2.0-85056353264
引用统计
文献类型	其他
条目标识符	https://kms.wmu.edu.cn/handle/3ETUA0LF/185514
专题	检验医学院（生命科学学院、生物学实验教学中心）检验医学院（生命科学学院、生物学实验教学中心）_Attardei线粒体研究院
通讯作者	Chen, Ye
作者单位	1.Zhejiang Univ, Childrens Hosp, Div Med Genet & Genom, Sch Med, Hangzhou 310003, Zhejiang, Peoples R China; 2.Zhejiang Univ, Inst Genet, Hangzhou 310058, Zhejiang, Peoples R China; 3.Wenzhou Med Univ, Attardi Inst Mitochondrial Biomed, Sch Lab Med & Life Sci, Wenzhou 325035, Peoples R China
推荐引用方式 GB/T 7714	Zheng, Jing,Meng, Wen-fang,Zhang, Chao-fan,等. New SNP variants of MARVELD2 (DFNB49) associated with non-syndromic hearing loss in Chinese population 中国人群中非综合征耳聋相关 MARVELD2 (DFNB49)基因新单核苷酸多态性位点分析. 2019.