A novel mutation in the HCN4 gene causes symptomatic sinus bradycardia in Moroccan Jews.

JOURNAL OF CARDIOVASCULAR ELECTROPHYSIOLOGY(2010)

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摘要
we describe a new mutation in the HCN4 gene causing symptomatic FSB in 3 unrelated individuals of similar ethnic background that may indicate unexplained FSB in this ethnic group. This profound functional defect is consistent with the symptomatic phenotype.
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关键词
electrophysiology,genetics,heart rate,ion channel
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