Original Research
Published on 20 Feb 2024
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
in Cardiac Rhythmology
![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](https://www.frontiersin.org/files/myhome article library/1320687/1320687_Thumb_400.jpg)
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