位置：成果数据库 > 期刊 > 期刊详情页
A novel variant in the 3' UTR of human SCN1A gene from a patient with Dravet syndrome decreases
  • ISSN号：0340-6717
  • 期刊名称：Hum Genet
  • 时间：2014
  • 页码：-
  • 相关项目：脆性X智力低下蛋白(FMRP)与miRNAs的相互调节机制及其可能的致病作用
作者： Zeng T, Dong ZF, Liu SJ, Wan RP, Tang LJ, Liu T,|
同期刊论文项目
脆性X智力低下蛋白(FMRP)与miRNAs的相互调节机制及其可能的致病作用
期刊论文 8
同项目期刊论文
A conserved region in the 3' untranslated region of the human LIMK1 gene is critical for pro
A microRNA profile in Fmr1 knockout mice reveals microRNA expression alterations with possible roles
Transcription of the Human Sodium Channel SCN1A Gene Is Repressed by a Scaffolding Protein RACK1.
A conserved region in the 3' untranslated region of the human LIMK1 gene is critical for proper
解读北美脆性X临床与研究协会临床实践共识——脆性X综合征药物治疗指南