Defective protein trafficking in hERG-associated hereditary long QT syndrome (LQT2): molecular mechanisms and restoration of intracellular protein processing
Open Access
- 1 November 2003
- journal article
- review article
- Published by Oxford University Press (OUP) in Cardiovascular Research
- Vol. 60 (2) , 235-241
- https://doi.org/10.1016/j.cardiores.2003.08.002
Abstract
Human hereditary long QT syndrome is a cardiac disease characterized by prolongation of the QT interval and increased susceptibility to ventricular aKeywords
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