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Further Insights in the Most Common SCN5A Mutation Causing Overlapping Phenotype of Long QT Syndrome, Brugada Syndrome, and Conduction Defect.
- Published in:
- 2016
- By:
- Publication type:
- journal article
Coexistence of atrioventricular accessory pathways and drug‐induced type 1 Brugada pattern.
- Published in:
- Pacing & Clinical Electrophysiology, 2018, v. 41, n. 9, p. 1078, doi. 10.1111/pace.13414
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- Publication type:
- Article
Dual Variation in SCN5A and CACNB2b Underlies the Development of Cardiac Conduction Disease without Brugada Syndrome.
- Published in:
- Pacing & Clinical Electrophysiology, 2010, v. 33, n. 3, p. 274, doi. 10.1111/j.1540-8159.2009.02642.x
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- Publication type:
- Article
LQT5 masquerading as LQT2: a dominant negative effect of KCNE1-D85N rare polymorphism on KCNH2 current.
- Published in:
- EP: Europace, 2011, v. 13, n. 10, p. 1478, doi. 10.1093/europace/eur184
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- Publication type:
- Article
Mutations in Na<sub>V</sub>1.5 Reveal Calcium-Calmodulin Regulation of Sodium Channel.
- Published in:
- Frontiers in Physiology, 2019, p. N.PAG, doi. 10.3389/fphys.2019.00700
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- Publication type:
- Article
Long QT, syndactyly, joint contractures, stroke and novel CACNA1C mutation: Expanding the spectrum of Timothy syndrome.
- Published in:
- American Journal of Medical Genetics. Part A, 2012, v. 158A, n. 1, p. 182, doi. 10.1002/ajmg.a.34355
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- Publication type:
- Article
De novo KCNQ1 mutation responsible for atrial fibrillation and short QT syndrome in utero
- Published in:
- Cardiovascular Research, 2005, v. 68, n. 3, p. 433, doi. 10.1016/j.cardiores.2005.06.023
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- Publication type:
- Article
Overlapping LQT1 and LQT2 phenotype in a patient with long QT syndrome associated with loss-of-function variations in KCNQ1 and KCNH2.
- Published in:
- Canadian Journal of Physiology & Pharmacology, 2010, v. 88, n. 12, p. 1181, doi. 10.1139/Y10-094
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- Publication type:
- Article