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学科主题临床医学
A novel 3017-bp deletion mutation in the FERMT1 (KIND1) gene in a Chinese family with Kindler syndrome
Zhou, C.1; Song, S.2; Zhang, J.1
关键词Deletion Mutation Fermt1 Kind1 Kindler Syndrome
刊名BRITISH JOURNAL OF DERMATOLOGY
2009-05-01
DOI10.1111/j.1365-2133.2009.09052.x
160期:5页:1119-1122
收录类别SCI
文章类型Letter
WOS标题词Science & Technology
类目[WOS]Dermatology
研究领域[WOS]Dermatology
关键词[WOS]PROTEIN ; KINDLIN-1 ; HOMOLOGY
语种英语
WOS记录号WOS:000265185500030
Citation statistics
Cited Times:11[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/400002259/57265
Collection北京大学第二临床医学院_皮科
作者单位1.Peking Univ, Dept Dermatol, Peoples Hosp, Beijing 100871, Peoples R China
2.Peking Univ, Hlth Sci Ctr, Dept Med Genet, Beijing 100083, Peoples R China
Recommended Citation
GB/T 7714
Zhou, C.,Song, S.,Zhang, J.. A novel 3017-bp deletion mutation in the FERMT1 (KIND1) gene in a Chinese family with Kindler syndrome[J]. BRITISH JOURNAL OF DERMATOLOGY,2009,160(5):1119-1122.
APA Zhou, C.,Song, S.,&Zhang, J..(2009).A novel 3017-bp deletion mutation in the FERMT1 (KIND1) gene in a Chinese family with Kindler syndrome.BRITISH JOURNAL OF DERMATOLOGY,160(5),1119-1122.
MLA Zhou, C.,et al."A novel 3017-bp deletion mutation in the FERMT1 (KIND1) gene in a Chinese family with Kindler syndrome".BRITISH JOURNAL OF DERMATOLOGY 160.5(2009):1119-1122.
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