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Paper Details

Heritability in a SCN5A-mutation founder population with increased female susceptibility to non-nocturnal ventricular tachyarrhythmia and sudden cardiac death.
Heart Rhythm
18
2017
4852delTCT, Brugada syndrome, Heritable, Phe1617del, SCN5A, SCN5A c.4850_4852delTCT, SCN5A-mutation, arrhythmia syndromes, cardiac, cardiac-sodium, cardiac-sodium channel dysfunction, conduction delay, identical, long-QT syndrome, non-nocturnal ventricular tachyarrhythmia, p.(Phe1617del, p.(Phe1617del), sodium, sudden cardiac death, ventricular fibrillation, ventricular tachyarrhythmias
Author NameAffiliation
Aaron IsaacsMaastricht University
Monika StollMaastricht University, Institute of Human Genetics, University of Munster
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Release 1.2