Loss-of-function mutations of the K+ channel gene KCNJ2 constitute a rare cause of long QT syndrome
- 1 August 2004
- journal article
- Published by Elsevier in Journal of Molecular and Cellular Cardiology
- Vol. 37 (2) , 593-602
- https://doi.org/10.1016/j.yjmcc.2004.05.011
Abstract
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