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Petitprez, S; Jespersen, T; Pruvot, E; Keller, D I; Corbaz, C; Schläpfer, J; Abriel, H; Kucera, J P (2008). Analysis of a novel SCN5A mutation (C1850S): conduction vs. repolarization disorder hypotheses in the Brugada syndrome. Cardiovascular research, 78(3), pp. 494-504. Oxford: Oxford University Press 10.1093/cvr/cvn023
Keller, D; Rougier, J; Kucera, J; Benammar, N; Fressart, V; Guicheney, P; Madle, A; Fromer, M; Schläpfer, J; Abriel, H (2005). Brugada syndrome and fever: Genetic and molecular characterization of patients carrying mutations. Cardiovascular research, 67(3), pp. 510-519. Oxford University Press 10.1016/j.cardiores.2005.03.024
