Epidemiologic, molecular, and functional evidence suggest A572D-SCN5A should not be considered an independent LQT3-susceptibility mutation.
第一作者:
David J,Tester
第一单位:
Department of Medicine, Mayo Clinic, Rochester, Minnesota, USA.
作者:
医学主题词
基因频率(Gene Frequency);疾病遗传易感性(Genetic Predisposition to Disease);遗传变异(Genetic Variation);人类(Humans);QT延长综合征(Long QT Syndrome);肌蛋白质类(Muscle Proteins);膜片钳术(Patch-Clamp Techniques);多态现象, 遗传(Polymorphism, Genetic);钠通道(Sodium Channels)
DOI
10.1016/j.hrthm.2010.04.014
PMID
20403459
发布时间
2025-05-29
- 浏览21
Heart rhythm
912-9页
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