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	An Intron Mutation in the ACVRL1 May Be Associated with a Transcriptional Regulation Defect in a Chinese Family with Hereditary Hemorrhagic Telangiectasia
	Yu, Qian; Shen, Xiao-Hui; Li, Ying; Li, Rui-Juan; Li, Ji; Luo, Yun-Ya; Liu, Su-Fang; Deng, Ming-Yang; Pei, Min-Fei; Zhang, Guang-Sen
刊名	PLOS ONE
	2013
卷号	8期号:2页码:e58031
关键词	Introns,Mutation,Polymerase chain reaction,Point mutation,Luciferase,Mutation detection,Electrophoretic mobility shift assay,DNA transcription
ISSN号	1932-6203
DOI	10.1371/journal.pone.0058031
URL标识	查看原文
WOS记录号	WOS:000315519000174
内容类型	期刊论文
URI标识	http://www.corc.org.cn/handle/1471x/3339795
专题	中南大学
作者单位	1.[Pei, Min-Fei 2.Luo, Yun-Ya 3.Li, Ying 4.Deng, Ming-Yang 5.Zhang, Guang-Sen 6.Yu, Qian 7.Shen, Xiao-Hui 8.Li, Rui-Juan 9.Liu, Su-Fang 10.Li, Ji] Cent S Univ, Xiang Ya Hosp 2, Inst Mol Hematol, Div Hematol, Changsha, Hunan, Peoples R China.
推荐引用方式 GB/T 7714	Yu, Qian,Shen, Xiao-Hui,Li, Ying,et al. An Intron Mutation in the ACVRL1 May Be Associated with a Transcriptional Regulation Defect in a Chinese Family with Hereditary Hemorrhagic Telangiectasia[J]. PLOS ONE,2013,8(2):e58031.
APA	Yu, Qian.,Shen, Xiao-Hui.,Li, Ying.,Li, Rui-Juan.,Li, Ji.,...&Zhang, Guang-Sen.(2013).An Intron Mutation in the ACVRL1 May Be Associated with a Transcriptional Regulation Defect in a Chinese Family with Hereditary Hemorrhagic Telangiectasia.PLOS ONE,8(2),e58031.
MLA	Yu, Qian,et al."An Intron Mutation in the ACVRL1 May Be Associated with a Transcriptional Regulation Defect in a Chinese Family with Hereditary Hemorrhagic Telangiectasia".PLOS ONE 8.2(2013):e58031.

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