Copy number variations of SCN5A in Brugada syndrome

Article ID	Journal	Published Year	Pages	File Type
8660106	Heart Rhythm	2018	32 Pages	PDF

Abstract

We identified SCN5A CNVs in 2.9% of BrS probands who were symptomatic or had a family history.

Keywords

SCN5A multiplex ligation-dependent probe amplification copy number variation duplication deletion Brugada syndrome

Related Topics

Health Sciences Medicine and Dentistry Cardiology and Cardiovascular Medicine

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Copy number variations of SCN5A in Brugada syndrome

Authors

Keiko MD, PhD, Seiko MD, PhD, Junichi MD, PhD, Mamoru MD, PhD, Tetsuhisa MD, PhD, Atsushi MD, PhD, Mitsuhiko MD, PhD, Isao MD, Seiichi MD, Yuichi MD, PhD, Takeru MD, PhD, Minoru MD, PhD,