Electrophysiological characterization of SCN5A mutations causing long QT (E1784K) and Brugada (R1512W and R1432G) syndromes
Open Access
- 1 April 2000
- journal article
- Published by Oxford University Press (OUP) in Cardiovascular Research
- Vol. 46 (1) , 55-65
- https://doi.org/10.1016/s0008-6363(00)00006-7
Abstract
Familial long QT syndrome (LQTS) and Brugada syndrome are two distinct human hereditary cardiac diseases known to cause ventricular tachyarrhythmiasKeywords
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