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Identification of a KCNE2 gain-of-function mutation in patients with familial atrial fibrillation.
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  • 相关项目：病理生理学
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病理生理学
期刊论文 15
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Mapping a Novel Locus for Familial Atrial Fibrillation on Chromosome 10p11-q21.
Spatial heterogeneity of muscarinic type 2 receptors in the atrium.
Kir2.3 knock-down decreases IK1 current in neonatal rat cardiomyocytes.
Refractoriness of the Sheep Superior Vena Cava Myocardial Sleeve.
High sensitivity of the sheep pulmonary vein antrum to acetylcholine stimulation.
Cardiac Electrophysiology in China.
A Kir2.1 gain-of-function mutation underlies familial atrial fibrillation.
GATA4基因突变与散发型先天性心脏病
NKX2—5基因与先天性心脏病的关系
心肌特异性表达人KCNE4转基因小鼠模型的建立
hKCNE5基因克隆及其重组腺病毒表达载体的构建
氯吡格雷和质子泵抑制剂联用的安全性