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Common Variants in Promoter of ADTRP Associate with Early-Onset Coronary Artery Disease in a Souther
  • 期刊名称：PLoS One
  • 时间：2015.10.1
  • 页码：e0137547-e0137547
  • 相关项目：中国人心脏钠离子通道病的病人特异性iPSCs来源心肌细胞的电生理学功能研究与SUNDS发病机制的新探索
作者： Lv GL|Zhao J|Cheng JD|Liu C|
同期刊论文项目
中国人心脏钠离子通道病的病人特异性iPSCs来源心肌细胞的电生理学功能研究与SUNDS发病机制的新探索
期刊论文 17
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青壮年猝死综合征钾离子通道KCNQ1、KCNH2、KCNE1和KCNE2基因的变异
Postmortem genetic screening of SNPs in RyR2 gene in sudden unexplained nocturnal death syndrome in
Association of common variants in NOS1AP gene with sudden unexplained nocturnal death syndrome in th
Is sudden unexplained nocturnal death syndrome in Southern China a cardiac sodium channel dysfunctio
Caveolin-3 suppresses late sodium current by inhibiting nNOS-dependent S-nitrosylation of SCN5A
青壮年不明原因夜间睡眠中猝死SCN5A基因型研究
A case-control study of sudden unexplained nocturnal death syndrome in the southern Chinese Han popu
Identification of rare variants of DSP gene in sudden unexplained nocturnal death syndrome in the so
Postmortem molecular analysis of KCNQ1, KCNH2, KCNE1 and KCNE2 genes in sudden unexplained nocturnal
Brugada综合征患者诱导性多能干细胞系的建立
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Ryanodine受体2和肌集钙蛋白2基因突变与儿茶酚胺敏感性多形性室性心动过速
云南猝死综合征的流行特征及其研究进展
SCN5A基因变异H558R携带者轻度心脏挫伤后死亡1例