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2008

I. Six, Hermida, J. - S., Huang, H., Gouas, L., Fressart, V., Benammar, N., Hainque, B., Denjoy, I., Chahine, M., and Guicheney, P., “The occurrence of Brugada syndrome and isolated cardiac conductive disease in the same family could be due to a single SCN5A mutation or to the accidental association of both diseases.”, Europace, vol. 10, no. 1, pp. 79-85, 2008.

2005

D. I. Keller, Barrane, F. - Z., Gouas, L., Martin, J., Pilote, S., Suarez, V., Osswald, S., Brink, M., Guicheney, P., Schwick, N., and Chahine, M., “A novel nonsense mutation in the SCN5A gene leads to Brugada syndrome and a silent gene mutation carrier state.”, Can J Cardiol, vol. 21, no. 11, pp. 925-31, 2005.

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