IndraLab
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"Mutations in Scn5a causing increased late I Na have been implicated to cause LQT3 [XREF_BIBR], and mutations causing decreased peak and early I Na have been implicated to cause a number of syndromes, including BrS, idiopathic ventricular fibrillation (IVF), cardiac conduction disease (CCD), sick sinus syndrome (SSS), and familial atrial fibrillation (FAF) [XREF_BIBR; XREF_BIBR]."