Associated Papers
SCN5A variant type-dependent risk prediction in Brugada syndrome.
Aizawa T et al.
Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups on Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology, 2025
39931825 (PubMed )
Supplement: euaf024_supplementary_data.pdf
Gene mutations in comorbidity of epilepsy and arrhythmia.
Yu C et al.
Journal of Neurology, 2023
The brain-heart interaction in epilepsy: implications for diagnosis, therapy, and SUDEP prevention.
Costagliola G et al.
Annals of Clinical and Translational Neurology, 2021
Variant frequencies of KCNQ1, KCNH2, and SCN5A in a Chinese inherited arrhythmia cohort and other disease cohorts undergoing genetic testing.
Li X et al.
Annals of Human Genetics, 2020
Coexistence of epilepsy and Brugada syndrome in a family with SCN5A mutation.
Parisi P et al.
Epilepsy Research, 2013
Novel isoforms of the sodium channels Nav1.8 and Nav1.5 are produced by a conserved mechanism in mouse and rat.
Kerr NC et al.
The Journal of Biological Chemistry, 2004
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