SCN5A mutation (T1620M) causing Brugada syndrome exhibits different phenotypes when expressed in Xenopus oocytes and mammalian cells
Open Access
- 2 February 2000
- journal article
- Published by Wiley in FEBS Letters
- Vol. 467 (1) , 12-16
- https://doi.org/10.1016/s0014-5793(00)01099-1
Abstract
Brugada syndrome is a hereditary cardiac disease causing abnormal ST segment elevation in the ECG, right bundle branch block, ventricular fibrillation and sudden death. In this study we characterized...Keywords
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