Normalization of Ventricular Repolarization with Flecainide in Long QT Syndrome Patients with SCN5A:ΔKPQ Mutation

Background: The Long QT Syndrome (LQTS) is a genetic channelopathy with life‐threatening implications. The LQT3 form of this disease is caused by mutations of the SCN5A sodium‐channel gene. A specific mutation, SCN5A:ΔKPQ, is associated with repetitive reopenings of the sodium channel and prolonged...

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Vydáno v:Ann Noninvasive Electrocardiol
Hlavní autoři: Windle, John R., Geletka, Robin C., Moss, Arthur J., Zareba, Wojciech, Atkins, Dianne L.
Médium: Artigo
Jazyk:Inglês
Vydáno: Blackwell Publishing Ltd 2006
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On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC7027642/
https://ncbi.nlm.nih.gov/pubmed/11333173
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/j.1542-474X.2001.tb00100.x
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