QQ客服 官方微博 反馈留言

	Noncanonical and canonical splice sites: a novel mutation at the rare noncanonical splice-donor cut site (IVS4+1A > G) of SEDL causes variable splicing isoforms in X-linked spondyloepiphyseal dysplasia tarda
	Xiong, Feng; Gao, Jianjun; Li, Jun; Liu, Yun; Feng, Guoyin; Fang, Wenli; Chang, Hongfen; Xie, Jiang; Zheng, Haitao; Li, Tingyu
刊名	EUROPEAN JOURNAL OF HUMAN GENETICS
	2009
卷号	17期号:4
关键词	alternative splicing canonical splice site mutation analysis noncanonical splice site splicing mechanism spondyloepiphyseal dysplasia tarda
ISSN号	1018-4813
URL标识	查看原文
语种	英语
内容类型	期刊论文
URI标识	http://www.corc.org.cn/handle/1471x/4949908
专题	复旦大学上海医学院
推荐引用方式 GB/T 7714	Xiong, Feng,Gao, Jianjun,Li, Jun,et al. Noncanonical and canonical splice sites: a novel mutation at the rare noncanonical splice-donor cut site (IVS4+1A > G) of SEDL causes variable splicing isoforms in X-linked spondyloepiphyseal dysplasia tarda[J]. EUROPEAN JOURNAL OF HUMAN GENETICS,2009,17(4).
APA	Xiong, Feng.,Gao, Jianjun.,Li, Jun.,Liu, Yun.,Feng, Guoyin.,...&He, Lin.(2009).Noncanonical and canonical splice sites: a novel mutation at the rare noncanonical splice-donor cut site (IVS4+1A > G) of SEDL causes variable splicing isoforms in X-linked spondyloepiphyseal dysplasia tarda.EUROPEAN JOURNAL OF HUMAN GENETICS,17(4).
MLA	Xiong, Feng,et al."Noncanonical and canonical splice sites: a novel mutation at the rare noncanonical splice-donor cut site (IVS4+1A > G) of SEDL causes variable splicing isoforms in X-linked spondyloepiphyseal dysplasia tarda".EUROPEAN JOURNAL OF HUMAN GENETICS 17.4(2009).

个性服务

查看访问统计

相关权益政策

暂无数据

收藏/分享

除非特别说明，本系统中所有内容都受版权保护，并保留所有权利。