Unravelling Novel ISCN5A/I Mutations Linked to Brugada Syndrome: Functional, Structural, and Genetic...
Unravelling Novel ISCN5A/I Mutations Linked to Brugada Syndrome: Functional, Structural, and Genetic Insights
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Author / Creator
Frosio, Anthony , Micaglio, Emanuele , Polsinelli, Ivan , Calamaio, Serena , Melgari, Dario , Prevostini, Rachele , Ghiroldi, Andrea , Binda, Anna , Carrera, Paola , Villa, Marco , Mastrocinque, Flavio , Presi, Silvia , Salerno, Raffaele , Boccellino, Antonio , Anastasia, Luigi , Ciconte, Giuseppe , Ricagno, Stefano , Pappone, Carlo and Rivolta, Ilaria
Publisher
MDPI AG
Journal title
Language
English
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Publication information
Publisher
MDPI AG
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Scope and Contents
Contents
Brugada Syndrome (BrS) is a rare inherited cardiac arrhythmia causing potentially fatal ventricular tachycardia or fibrillation, mainly occurring during rest or sleep in young individuals without heart structural issues. It increases the risk of sudden cardiac death, and its characteristic feature is an abnormal ST segment elevation on the ECG. Whi...
Alternative Titles
Full title
Unravelling Novel ISCN5A/I Mutations Linked to Brugada Syndrome: Functional, Structural, and Genetic Insights
Authors, Artists and Contributors
Author / Creator
Micaglio, Emanuele
Polsinelli, Ivan
Calamaio, Serena
Melgari, Dario
Prevostini, Rachele
Ghiroldi, Andrea
Binda, Anna
Carrera, Paola
Villa, Marco
Mastrocinque, Flavio
Presi, Silvia
Salerno, Raffaele
Boccellino, Antonio
Anastasia, Luigi
Ciconte, Giuseppe
Ricagno, Stefano
Pappone, Carlo
Rivolta, Ilaria
Identifiers
Primary Identifiers
Record Identifier
TN_cdi_gale_infotracmisc_A771910190
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_gale_infotracmisc_A771910190
Other Identifiers
ISSN
1422-0067
DOI
10.3390/ijms242015089
