Ranolazine as an Alternative Therapy to Flecainide for SCN5A V411M Long QT Syndrome Type 3 Patients

The prolongation of the QT interval represents the main feature of the long QT syndrome (LQTS), a life-threatening genetic disease. The heterozygous SCN5A V411M mutation of the human sodium channel leads to a LQTS type 3 with severe proarrhythmic effects due to an increase in the late component of t...

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Main Authors: Jordi Cano (Author), Esther Zorio (Author), Andrea Mazzanti (Author), Miguel Ángel Arnau (Author), Beatriz Trenor (Author), Silvia G. Priori (Author), Javier Saiz (Author), Lucia Romero (Author)
Format: Book
Published: Frontiers Media S.A., 2020-12-01T00:00:00Z.
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3rd Floor Main Library

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Call Number: A1234.567
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