Genotype-phenotype correlation of rare variants in the SCN5A gene in children population

FUNDING ACKNOWLEDGEMENTS: Type of funding sources: None. BACKGROUND: Rare variants in the SCN5A gene have been associated with Brugada syndrome (BS), long QT syndrome type 3 (LQTS3), and other conduction disorders that can lead to life-threatening arrhythmias. Variable expressivity, incomplete penet...

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Detalles Bibliográficos
Autores principales: Martinez Barrios, E, Sarquella Brugada, G, Cruzalegui Gomez, J, Cesar Diaz, S, Chipa Ccasani, F, Greco, A, Fiol, V, Cerralbo, P, Brugada Terradellas, J, Campuzano Larrea, O
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
9.1.2 - Genetic Aspects of Arrhythmias
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10207523/
http://dx.doi.org/10.1093/europace/euad122.601

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10207523/
http://dx.doi.org/10.1093/europace/euad122.601

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