Nature · 1995 · 967 citations · 20 references
MedicineCardiologyMolecular GeneticsCardiovascular GeneticsElectrophysiologyHuman GeneticsCardiac ArrhythmiasCardiac Conduction SystemCardiac Ion ChannelsInherited Arrhythmia SyndromesInherited CardiomyopathiesSudden Cardiac Death GeneticsArrhythmogenic MechanismsElectrophysiological PhenotypingInherited Cardiac ChannelopathiesInherited Channelopathy-related Ventricular Tachycardia
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A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome
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SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome
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Structural parts involved in activation and inactivation of the sodium channel
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