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钠离子通道SCN5A基因突变与遗传性心脏病研究进展 被引量：1

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摘要 大量研究表明，钠离子通道在维持心肌细胞的正常功能上发挥着重要的作用，心脏钠离子通道SCN5A基因突变可致多种心脏疾病，其中遗传性室性心律失常就是目前研究较多的一大类疾病，如长QT综合征（LQTS）、Brugada综合征、特发性心室颤动、婴儿猝死综合征等，本综述主要报道SCN5A基因与遗传性室性心律失常类疾病。
作者 龚红霞 白亚娜 胡晓斌 程宁
机构地区 兰州大学公共卫生学院流行病与卫生统计研究所 兰州大学生殖健康与出生缺陷研究中心
出处 《心电学杂志》 2011年第3期255-258,共4页 Journal of Electrocardiology(China)
基金 兰州大学中央高校基本科研业务专项资金（LZUJBKJ-2009-91）：兰州大学交叉学科青年创新研究基金（LZU-JC200920）
关键词 SCN5A基因突变 遗传性心脏病 钠离子通道 遗传性室性心律失常 Brugada综合征 特发性心室颤动 婴儿猝死综合征 心脏疾病
分类号 R541.7 [医药卫生—心血管疾病]
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参考文献25

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共引文献23

同被引文献13

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心电学杂志
2011年 第3期

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