Beneficial normalization of cardiac repolarization by carnitine in transgenic short QT syndrome type 1 rabbit models
{{output}}
Aims: Short QT syndrome type 1 (SQT1) is a genetic channelopathy caused by gain-of-function variants in human-ether-a-go-go (HERG) underlying the rapid delayed-rectifier K+ current (IKr), leading to QT-shortening, ventricular arr... ...
