锚蛋白基因突变与心肌离子通道病
摘要
心肌离子通道病（cardiac ion channelopathies）是由编码心肌细胞膜离子通道及其相关蛋白的基因发生突变，使其表达和／或膜定位异常，通道的功能出现不同程度的削弱或增强所导致的一组机体整体生理功能紊乱的综合征。体内出现针对通道的内源性病理性物质时，亦可导致离子通道病。因其病因基础在细胞膜的分子水平.
出处
《临床急诊杂志》
CAS
2007年第3期185-187,共3页
Journal of Clinical Emergency
基金
深圳市重点医学专科(2005-25-C13
2005-25-C09)
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