Pediatric Malignant Arrhythmias Caused by Rare Homozygous Genetic Variants in TRDN: A Comprehensive Interpretation

• Main Authors: Georgia Sarquella-Brugada (Author), Anna Fernandez-Falgueras (Author), Sergi Cesar (Author), Elena Arbelo (Author), Paloma Jordà (Author), Ana García-Álvarez (Author), Jose Carlos Cruzalegui (Author), Erika Fernanda Merchan (Author), Victoria Fiol (Author), Josep Brugada (Author), Ramon Brugada (Author), Oscar Campuzano (Author)
• Format: Book
• Published: Frontiers Media S.A., 2021-02-01T00:00:00Z.
• Subjects: article
• Online Access: Connect to this object online.

Aim: To perform a comprehensive phenotype-genotype correlation of all rare variants in Triadin leading to malignant arrhythmias in pediatrics.Methods: Triadin knockout syndrome is a rare entity reported in pediatric population. This syndrome is caused by rare variants in the TRDN gene. Malignant ven...