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Novel SCN5A Mutation Leading Either to Isolated Cardiac Conduction Defect or Brugada Syndrome in a Large French Family
Kyndt, F., Probst, V., Potet, F., Demolombe, S., Chevallier, J.-C., Baro, I., Moisan, J.-P., Boisseau, P., Schott, J.-J., Escande, D., Le Marec, H.Volume:
104
Language:
english
Journal:
Circulation
DOI:
10.1161/hc5001.100834
Date:
December, 2001
File:
PDF, 454 KB
english, 2001