Brugada syndrome is an inherited disease closely associated with genetic mutations,
resulting in ventricular fibrillation and sudden cardiac death. To date, more than 40 genes …

Brugada syndrome is a rare, inherited cardiac disease leading to ventricular fibrillation and
sudden cardiac death in structurally normal hearts. Clinical diagnosis requires a Brugada …

Brugada syndrome is a rare inherited arrhythmogenic disease leading to ventricular
fibrillation and high risk of sudden death. In 1998, this syndrome was linked with a genetic …

Brugada syndrome (BrS) is diagnosed by a coved-type ST-segment elevation in the right
precordial leads on the electrocardiogram (ECG), and it is associated with an increased risk …

Brugada syndrome (BrS) is a known cause of sudden cardiac death. The genetic basis of
BrS is not well understood, and no one single gene is linked to even a majority of BrS cases …

For the last 10 years, applying new sequencing technologies to thousands of whole exomes
has revealed the high variability of the human genome. Extreme caution should thus be …

Brugada syndrome is a rare cardiac arrhythmia characterized by electrocardiographic right
bundle branch block and persistent ST-segment elevation in the right precordial leads. It is …

Brugada syndrome (BrS) is diagnosed by the presence of an elevated ST-segment and can
result in sudden cardiac death. The most commonly found mutated gene is SCN5A, which …

Brugada syndrome (BrS) is an inherited electrical heart disease associated with a high risk
of sudden cardiac death (SCD). The genetic characterization of BrS has always been …

Brugada syndrome (BrS) is an inherited cardiac arrhythmic disorder that can lead to sudden
death, with a prevalence of 1: 5000 in Caucasian population and affecting mainly male …