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Identification of a novel Scn3b mutation in a Chinese Brugada syndrome pedigree: implications for Nav1.5 electrophysiological properties and intracellular distribution of Nav1.5 and Navβ3.
- Published in:
- Frontiers in Cardiovascular Medicine, 2024, p. 01, doi. 10.3389/fcvm.2024.1320687
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- Article