Items where Author is "Abriel, H."
Jump to: 2008
Number of items: 1.
Petitprez, S. and Jespersen, T. and Pruvot, E. and Keller, D. I. and Corbaz, C. and Schläpfer, J. and Abriel, H. and Kucera, J. P.. (2008) Analyses of a novel SCN5A mutation (C1850S) : conduction vs : repolarization disorder hypotheses in the Brugada syndrome. Cardiovascular research, Vol. 78. S. 494-504.