Genetic testing of patients with long QT syndrome

Congenital long QT syndrome is mainly caused by mutations in the KCNQ1, KCNH2 and SCN5A genes. The aim of this study was to investigate the prevalence of mutations in these three genes in patients with long QT syndrome or idiopathic ventricular fibrillation seen at our center. The study included nin...

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Veröffentlicht in:	Revista española de cardiologia 2011-01, Vol.64 (1), p.71-74
Hauptverfasser:	Jiménez-Jáimez, Juan, Tercedor-Sánchez, Luis, Alvarez-López, Miguel, Martínez-Espín, Esther, Sebastián Galdeano, Ricardo, Almansa-Valencia, Isabel, Lorente, José A, Melgares-Moreno, Rafael
Format:	Artikel
Sprache:	eng
Online-Zugang:	Volltext
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