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Novel mutations in the vWFA2 domain of COCH in two Chinese DFNA9 families
Yuan, H. J.2; Han, D. Y.2; Sun, Q.2; Yan, D.1; Sun, H. J.2; Tao, R.3; Cheng, J.2; Qin, W.; Angeli, S.1; Ouyang, X. M.1; Yang, S. Z.2; Feng, L.4; Cao, J. Y.2; Feng, G. Y.3; Wang, Y. F.4; Dai, P.2; Zhai, S. Q.2; Yang, W. Y.2; He, L.3; Liu, X. Z.1
刊名CLINICAL GENETICS
2008-04-01
DOI10.1111/j.1399-0004.2008.00972.x
73期:4页:391-394
收录类别SCI
文章类型Letter
WOS标题词Science & Technology
类目[WOS]Genetics & Heredity
研究领域[WOS]Genetics & Heredity
关键词[WOS]PROGRESSIVE HEARING-LOSS ; MENIERES-DISEASE ; GENE ; DYSFUNCTION ; DEAFNESS
语种英语
WOS记录号WOS:000253977900017
Citation statistics
Cited Times:14[WOS]   [WOS Record]     [Related Records in WOS]
文献类型期刊论文
条目标识符http://ir.bjmu.edu.cn/handle/400002259/66491
Collection北京大学精神卫生研究所
作者单位1.Univ Miami, Dept Otolaryngol, D 48, Miami, FL 33136 USA
2.Chinese Peoples Liberat Army Gen Hosp, Inst Otolaryngol, Beijing, Peoples R China
3.Shanghai Jiao Tong Univ, BioX Life Sci Res Ctr, Shanghai 200030, Peoples R China
4.Peking Univ, Inst Mental Hlth, Beijing 100871, Peoples R China
Recommended Citation
GB/T 7714
Yuan, H. J.,Han, D. Y.,Sun, Q.,et al. Novel mutations in the vWFA2 domain of COCH in two Chinese DFNA9 families[J]. CLINICAL GENETICS,2008,73(4):391-394.
APA Yuan, H. J..,Han, D. Y..,Sun, Q..,Yan, D..,Sun, H. J..,...&Liu, X. Z..(2008).Novel mutations in the vWFA2 domain of COCH in two Chinese DFNA9 families.CLINICAL GENETICS,73(4),391-394.
MLA Yuan, H. J.,et al."Novel mutations in the vWFA2 domain of COCH in two Chinese DFNA9 families".CLINICAL GENETICS 73.4(2008):391-394.
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