Defective cardiac ion channels: from mutations to clinical syndromes
Author:
Publisher
American Society for Clinical Investigation
Subject
General Medicine
Reference23 articles.
1. Two Distinct Congenital Arrhythmias Evoked by a Multidysfunctional Na + Channel
2. Inherited Brugada and Long QT-3 Syndrome Mutations of a Single Residue of the Cardiac Sodium Channel Confer Distinct Channel and Clinical Phenotypes
3. Long QT syndrome, Brugada syndrome, and conduction system disease are linked to a single sodium channel mutation
4. A Single Na + Channel Mutation Causing Both Long-QT and Brugada Syndromes
5. A sodium-channel mutation causes isolated cardiac conduction disease
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