Aya Miyazaki et al. JACEP 2016;2:

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Date of download: 6/25/2016 Copyright © The American College of Cardiology. All rights reserved. From: Sinus node function and ventricular repolarization.

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Aya Miyazaki et al. JACEP 2016;2:266-276 Locations of the Gene Mutations in 8 Perinatal LQTS Patients With Neurological Comorbidities The upper and lower figures show the predicted topology of the Kv11.1 cardiac potassium channel α-subunit and the Nav1.5 cardiac sodium channel α-subunit, respectively. The pink solid circles indicate the mutations in patients with perinatal long QT syndrome (LQTS) with epilepsy and/or developmental disorders from our institution. The blue solid circle indicates the mutation in a previously reported case of perinatal LQTS and neurological seizures. Aya Miyazaki et al. JACEP 2016;2:266-276 American College of Cardiology Foundation