CORC  > 复旦大学上海医学院
Rare mutations in apoptosis related genes APAF1, CASP9, and CASP3 contribute to human neural tube defects
Zhou, Xiangyu; Zeng, Weijia; Li, Huili; Chen, Haitao; Wei, Gang; Yang, Xueyan; Zhang, Ting; Wang, Hongyan
刊名CELL DEATH & DISEASE
2018
卷号9
ISSN号2041-4889
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/3601852
专题复旦大学上海医学院
推荐引用方式
GB/T 7714
Zhou, Xiangyu,Zeng, Weijia,Li, Huili,et al. Rare mutations in apoptosis related genes APAF1, CASP9, and CASP3 contribute to human neural tube defects[J]. CELL DEATH & DISEASE,2018,9.
APA Zhou, Xiangyu.,Zeng, Weijia.,Li, Huili.,Chen, Haitao.,Wei, Gang.,...&Wang, Hongyan.(2018).Rare mutations in apoptosis related genes APAF1, CASP9, and CASP3 contribute to human neural tube defects.CELL DEATH & DISEASE,9.
MLA Zhou, Xiangyu,et al."Rare mutations in apoptosis related genes APAF1, CASP9, and CASP3 contribute to human neural tube defects".CELL DEATH & DISEASE 9(2018).
个性服务
查看访问统计
相关权益政策
暂无数据
收藏/分享
所有评论 (0)
暂无评论
 

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。


©版权所有 ©2017 CSpace - Powered by CSpace