Syntrophin mutation associated with long QT syndrome through activation of the nNOS-SCN5A macromolecular complex
Author:
Publisher
Proceedings of the National Academy of Sciences
Subject
Multidisciplinary
Reference28 articles.
1. Inherited Arrhythmias
2. Regulation of the Voltage-Gated Cardiac Sodium Channel Nav1.5 by Interacting Proteins
3. Mutant Caveolin-3 Induces Persistent Late Sodium Current and Is Associated With Long-QT Syndrome
4. SCN4B -Encoded Sodium Channel β4 Subunit in Congenital Long-QT Syndrome
5. Mutation of an A-kinase-anchoring protein causes long-QT syndrome
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