Genetic testing in children with Brugada syndrome: results from a large prospective registry

AIMS: A pathogenic/likely pathogenic (P/LP) variant in SCN5A is found in 20–25% of patients with Brugada syndrome (BrS). However, the diagnostic yield and prognosis of gene panel testing in paediatric BrS is unclear. The aim of this study is to define the diagnostic yield and outcomes of SCN5A gene...

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Detalles Bibliográficos
Autores principales: Pannone, Luigi, Bisignani, Antonio, Osei, Randy, Gauthey, Anaïs, Sorgente, Antonio, Vergara, Pasquale, Monaco, Cinzia, Della Rocca, Domenico Giovanni, Del Monte, Alvise, Strazdas, Antanas, Mojica, Joerelle, Al Housari, Maysam, Miraglia, Vincenzo, Mouram, Sahar, Paparella, Gaetano, Ramak, Robbert, Overeinder, Ingrid, Bala, Gezim, Almorad, Alexandre, Ströker, Erwin, Pappaert, Gudrun, Sieira, Juan, de Ravel, Thomy, La Meir, Mark, Brugada, Pedro, Chierchia, Gian Battista, Van Dooren, Sonia, de Asmundis, Carlo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Clinical Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10227762/
https://www.ncbi.nlm.nih.gov/pubmed/37061847
http://dx.doi.org/10.1093/europace/euad079

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10227762/
https://www.ncbi.nlm.nih.gov/pubmed/37061847
http://dx.doi.org/10.1093/europace/euad079

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