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J.HRTHM.2009.02.009
J.HRTHM.2009.02.009
http://dx.doi.org/10.1016/J.HRTHM.2009.02.009
Mechanisms and clinical management of inherited channelopathies: long QT syndrome, Brugada syndrome, catecholaminergic polymorphic ventricular tachycardia, and short QT syndrome.
P356
Q33157630-878EA978-E590-4AB4-AF52-C61B82AA56E2
P356
J.HRTHM.2009.02.009
http://dx.doi.org/10.1016/J.HRTHM.2009.02.009