Experimental Models of Brugada syndrome

Experimental Models of Brugada syndrome

Brugada syndrome is an inherited, rare cardiac arrhythmogenic disease, associated with sudden cardiac death. It accounts for up to 20% of sudden deaths in patients without structural cardiac abnormalities. The majority of mutations involve the cardiac sodium channel gene <i>SCN5A</i> and...

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Bibliographic Details
Main Authors: Franziska Sendfeld, Elisabet Selga, Fabiana S. Scornik, Guillermo J. Pérez, Nicholas L. Mills, Ramon Brugada
Format: Article
Language:English
Published: MDPI AG 2019-04-01
Series:International Journal of Molecular Sciences
Subjects:
Brugada syndrome
<i>SCN5A</i>
model systems
induced pluripotent stem cells (iPS)
Online Access:https://www.mdpi.com/1422-0067/20/9/2123

Internet

https://www.mdpi.com/1422-0067/20/9/2123

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