KCNQ1 mutations in patients with a family history of lethal cardiac arrhythmias and sudden death
- 22 April 2003
- journal article
- research article
- Published by Wiley in Clinical Genetics
- Vol. 63 (4) , 273-282
- https://doi.org/10.1034/j.1399-0004.2003.00048.x
Abstract
Long QT syndrome (LQTS) is the prototype of the cardiac ion channelopathies which cause syncope and sudden death. LQT1, due to mutations of KCNQ1 (KVLQT1), is the most common form. This study describ...Keywords
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