Referenced in: none

Automatically associated channels: Nav1.5 , Slo1

Title: SCN5A mutation (T1620M) causing Brugada syndrome exhibits different phenotypes when expressed in Xenopus oocytes and mammalian cells.

Authors: G Baroudi, E Carbonneau, V Pouliot, M Chahine

Journal, date & volume: FEBS Lett., 2000 Feb 4 , 467, 12-6

PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/10664447

Abstract