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Journal of Cardiology|March 25, 2017
Andersen-Tawil syndrome: Clinical presentation and predictors of symptomatic arrhythmias - Possible role of polymorphisms K897T in KCNH2 and H558R in SCN5A geneMichalina Krych, Elżbieta Katarzyna Biernacka, Joanna Ponińska, et al.
Journal of Cardiovascular Electrophysiology|September 15, 2016
Disappearance of Idiopathic Outflow Tract Premature Ventricular Contractions After Catheter Ablation of Overt Accessory PathwaysTamas Szili Torok, Lennart J DE Vries, Emin E Özcan, et al.
Circulation|March 17, 2004
Relation between pulmonary vein firing and extent of left atrial-pulmonary vein connection in patients with atrial fibrillationHiroshi Nakagawa, Hiroshi Aoyama, Karen J Beckman, et al.
Pacing and Clinical Electrophysiology : PACE|June 29, 2018
Coexistence of atrioventricular accessory pathways and drug-induced type 1 Brugada patternCan Hasdemir, Jimmy Jyh-Ming Juang, Sedat Kose, et al.
Frontiers in Physiology|November 6, 2025
Case Report: Loss-of-function TRPM4 mutation p.L91Δ implicated in progressive cardiac conduction defectAnne-Flore Hämmerli, Daniela Ross-Kaschitza, Prakash Arullampalam, et al.
The Journal of Clinical Investigation|May 10, 2008
Sodium channel β1 subunit mutations associated with Brugada syndrome and cardiac conduction disease in humansHiroshi Watanabe, Tamara T Koopmann, Solena Le Scouarnec, et al.
Circulation. Arrhythmia and Electrophysiology|January 17, 2012
A connexin40 mutation associated with a malignant variant of progressive familial heart block type INaomasa Makita, Akiko Seki, Naokata Sumitomo, et al.
JACC. Clinical Electrophysiology|April 17, 2026
Biophysical Characterization of a Novel KCNJ8 Rare Variant Linked With Inherited and Acquired J Wave SyndromeDan Hu, Yan Huang, Cinthia Rangel-Sandoval, et al.
Journal of the American College of Cardiology|July 7, 2014
Mutations in SCN10A are responsible for a large fraction of cases of Brugada syndromeDan Hu, Hector Barajas-Martínez, Ryan Pfeiffer, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 7, 2020
Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controlsRoddy Walsh, Najim Lahrouchi, Rafik Tadros, et al.
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