Publications
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Filters: Author is Berthet, M [Clear All Filters]
, “Homozygous SCN5A mutation in long-QT syndrome with functional two-to-one atrioventricular block.”, Circ Res, vol. 89, no. 2, pp. E16-21, 2001.
, “Electrophysiological characterization of SCN5A mutations causing long QT (E1784K) and Brugada (R1512W and R1432G) syndromes.”, Cardiovasc Res, vol. 46, no. 1, pp. 55-65, 2000.
