Population
Patients with or suspected of having Brugada syndrome and their family members
Design
Review
Authors
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Refines BrS diagnosis via right precordial lead placement; leaves open optimal SCD risk stratification in asymptomatic patients.
This review summarizes the genetic background of Brugada syndrome, highlighting SCN5A as the most common associated gene and discussing the role of genetic screening in clinical practice.
Juang et al. (2016) studied this question.
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