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