在线客服: 点击这里给我发消息  新用户使用步骤:会员注册→充值→重新登入→进入资源
标题:Compound heterozygous CACNA1H mutations associated with severe congenital amyotrophy.
时间:2019-11-18 17:34:09
DOI:10.1080/19336950.2019.1614415
PMID:31070086
作者:Melissa T Carter;Hugh J Mcmillan;Andriy Tomin
出版源: Channels (Austin, Tex.) ,2019 ,19 (1) :153-161
大小:3181 kb
页数:11 PAGES
下载: 点击下载
预览:

浏览器不支持嵌入PDF阅读,打开新页面在线阅读

目录:
  • Abstract
  • Introduction
  • Materials and methods
    • Whole exome sequencing
    • Plasmid cDNA constructs
    • Cell culture and heterologous expression
  • Recording of T-type currents
    • Statistical analysis
  • Results
    • Clinical characteristics and genetic analysis
    • Expression of Cav3.2 channel variants
    • Gating properties of Cav3.2 channel variants
    • Window current of Cav3.2 channel variants
  • Discussion
  • Acknowledgments
  • Disclosure statement
  • Funding
  • References

本页内容由网络收集而来,版权归原创者所有,如有侵权请及时联系