Associated Papers
Cardiac Channelopathies: Clinical Diagnosis and Promising Therapeutics.
Dib Nehme R et al.
Journal of the American Heart Association, 2025
Primary Electrical Heart Disease-Principles of Pathophysiology and Genetics.
Badura K et al.
International Journal of Molecular Sciences, 2024
Association of Cardiac Electrical Disorders With KCND3 Gene Mutation.
Ahammed MR et al.
Cureus, 2023
Cardiocerebral channelopathy caused by KCND3 mutation in a child: A case report.
Zhang Y et al.
Frontiers in Pediatrics, 2022
Rare Gain-of-Function KCND3 Variant Associated with Cerebellar Ataxia, Parkinsonism, Cognitive Dysfunction, and Brain Iron Accumulation.
Hsiao CT et al.
International Journal of Molecular Sciences, 2021
Towards Mutation-Specific Precision Medicine in Atypical Clinical Phenotypes of Inherited Arrhythmia Syndromes.
Nakajima T et al.
International Journal of Molecular Sciences, 2021
Novel Cardiocerebral Channelopathy Associated with a KCND3 V392I Mutation.
Nakajima T et al.
International Heart Journal, 2020
Inter-Regulation of Kv4.3 and Voltage-Gated Sodium Channels Underlies Predisposition to Cardiac and Neuronal Channelopathies.
Clatot J et al.
International Journal of Molecular Sciences, 2020
Heritable arrhythmias associated with abnormal function of cardiac potassium channels.
Crotti L et al.
Cardiovascular Research, 2020
A de novo gain-of-function KCND3 mutation in early repolarization syndrome.
Takayama K et al.
Heart Rhythm, 2019
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