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Analyses of a novel SCN5A mutation (C1850S): conduction vs. repolarization disorder hypotheses in the Brugada syndrome.
Séverine Petitprez, Thomas Jespersen, Etienne Pruvot, Dagmar I Keller, Cora Corbaz, Jürg Schläpfer, Hugues Abriel, Jan P Kucera