Clinical Spectrum of SCN5A Channelopathy in Children with Primary Electrical Disease and Structurally Normal Hearts

Sodium voltage-gated channel α subunit 5 (SCN5A)-mutations may cause an array of arrhythmogenic syndromes most frequently as an autosomal dominant trait, with incomplete penetrance, variable expressivity and male predominance. In the present study, we retrospectively describe a group of Mexican pati...

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Detalles Bibliográficos
Autores principales: Villarreal-Molina, Teresa, García-Ordóñez, Gabriela Paola, Reyes-Quintero, Álvaro E., Domínguez-Pérez, Mayra, Jacobo-Albavera, Leonor, Nava, Santiago, Carnevale, Alessandra, Medeiros-Domingo, Argelia, Iturralde, Pedro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8774384/
https://www.ncbi.nlm.nih.gov/pubmed/35052356
http://dx.doi.org/10.3390/genes13010016

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8774384/
https://www.ncbi.nlm.nih.gov/pubmed/35052356
http://dx.doi.org/10.3390/genes13010016

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