Hipsc-Derived Cardiomyocyte Model of LQT2 Syndrome Derived from Asymptomatic and Symptomatic Mutation Carriers Reproduces Clinical Differences in Aggregates but Not in Single Cells.
Cells（2020）
Key words
HERG,LQT2,channelopathies,in vitro electrophysiology,arrhythmia,induced pluripotent stem cells,in-silico modeling
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