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Cardiomyocyte Deletion of Bmal1 Exacerbates QT- and RR-Interval Prolongation in Scn5a <sup>+/Δ KPQ </sup> Mice.
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- Frontiers in Physiology, 2021, v. 12, p. 1, doi. 10.3389/fphys.2021.681011
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- Article
Mutation-Specific Differences in Kv7.1 (KCNQ1) and Kv11.1 (KCNH2) Channel Dysfunction and Long QT Syndrome Phenotypes.
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- International Journal of Molecular Sciences, 2022, v. 23, n. 13, p. 7389, doi. 10.3390/ijms23137389
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- Article
A KCNQ1 Mutation Causes a High Penetrance for Familial Atrial Fibrillation.
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- Journal of Cardiovascular Electrophysiology, 2013, v. 24, n. 5, p. 562, doi. 10.1111/jce.12068
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- Article
Molecular pathogenesis of long QT syndrome type 2.
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- Journal of Arrhythmia, 2016, v. 32, n. 5, p. 373, doi. 10.1016/j.joa.2015.11.009
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- Article
Long QT Syndrome Type 2: Emerging Strategies for Correcting Class 2 KCNH2 (hERG) Mutations and Identifying New Patients.
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- Biomolecules (2218-273X), 2020, v. 10, n. 8, p. 1144, doi. 10.3390/biom10081144
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- Article
Divergent action potential morphologies reveal nonequilibrium properties of human cardiac Na channels
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- Cardiovascular Research, 2004, v. 64, n. 3, p. 477, doi. 10.1016/j.cardiores.2004.07.014
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- Article
Caution: merging ion channel traffic ahead.
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- Journal of Physiology, 2023, v. 601, n. 13, p. 2541, doi. 10.1113/JP284497
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- Article
The role of the cardiomyocyte circadian clocks in ion channel regulation and cardiac electrophysiology.
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- Journal of Physiology, 2022, v. 600, n. 9, p. 2037, doi. 10.1113/JP282402
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- Article