Brugada Syndrome: Oligogenic or Mendelian Disease?

Brugada Syndrome: Oligogenic or Mendelian Disease?

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 of sudden cardiac death (SCD) compared to the general population. Although BrS is considered a genetic disease, its molec...

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Bibliographic Details
Main Authors: Michelle M. Monasky, Emanuele Micaglio, Giuseppe Ciconte, Carlo Pappone
Format: Article
Language:English
Published: MDPI AG 2020-03-01
Series:International Journal of Molecular Sciences
Subjects:
brugada syndrome
sudden cardiac death
genetic testing
mutation
<i>scn5a</i>
sodium channel
arrhythmia
channelopathy
segregation analysis
functional studies
Online Access:https://www.mdpi.com/1422-0067/21/5/1687

Internet

https://www.mdpi.com/1422-0067/21/5/1687

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