Authors:
Lupoglazoff, JM
Cheav, T
Baroudi, G
Berthet, M
Denjoy, L
Cauchemez, B
Extramiana, F
Chahine, M
Guicheney, P
Citation: Jm. Lupoglazoff et al., Homozygous SCN5A mutation in long-QT syndrome with functional two-to-one atrioventricular block, CIRCUL RES, 89(2), 2001, pp. E16-E21
Citation: G. Baroudi et M. Chahine, Biophysical phenotypes of SCN5A mutations causing long QT and Brugada syndromes, FEBS LETTER, 487(2), 2000, pp. 224-228
Authors:
Baroudi, G
Carbonneau, E
Pouliot, V
Chahine, M
Citation: G. Baroudi et al., SCN5A mutation (T1620M) causing Brugada syndrome exhibits different phenotypes when expressed in Xenopus oocytes and mammalian cells, FEBS LETTER, 467(1), 2000, pp. 12-16
Authors:
Deschenes, I
Baroudi, G
Berthet, M
Barde, I
Chalvidan, T
Denjoy, I
Guicheney, P
Chahine, M
Citation: I. Deschenes et al., Electrophysiological characterization of SCN5A mutations causing long QT (E1784K) and Brugada (R1512W and R1432G) syndromes, CARDIO RES, 46(1), 2000, pp. 55-65