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Mutations in <i>MYBPC3</i> and <i>MYH7</i> in Association with Brugada Type 1 ECG Pattern: Overlap between Brugada Syndrome and Hypertrophic Cardiomyopathy?

Brugada syndrome (BrS) is an inherited disorder with high allelic and genetic heterogeneity clinically characterized by typical coved-type ST segment elevation at the electrocardiogram (ECG), which may occur either spontaneously or after provocative drug testing. BrS is classically described as an a...

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Uloženo v:
Hlavní autoři: Marianna Farnè, Cristina Balla, Alice Margutti, Rita Selvatici, Martina De Raffele, Assunta Di Domenico, Paola Imbrici, Elia De Maria, Mauro Biffi, Matteo Bertini, Claudio Rapezzi, Alessandra Ferlini, Francesca Gualandi
Médium: Artigo
Jazyk:Inglês
Vydáno: MDPI AG 2021-09-01
Edice:Cardiogenetics
Témata:
Brugada syndrome
overlapping phenotypes
sarcomeric genes
<i>MYBPC3</i>
<i>MYH7</i>
hypertrophic cardiomyopathy
On-line přístup:https://www.mdpi.com/2035-8148/11/3/16
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