Mutational spectrum of congenital long QT syndrome in Turkey; identification of 12 novel mutations across KCNQ1, KCNH2, SCN5A, KCNJ2, CACNA1C, and CALM1
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DOI: 10.1111/jce.15306
Abstract: Long QT syndrome (LQTS) is of great importance as it is the most common cause of sudden cardiac death in childhood. The diagnosis is made by the prolongation of the QTc interval on the electrocardiography.… read more here.
Keywords: long syndrome; spectrum congenital; syndrome turkey; congenital long ... See more keywords