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

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 ve...

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Detaylı Bibliyografya
Yayımlandı:Front Pediatr
Asıl Yazarlar: Sarquella-Brugada, Georgia, Fernandez-Falgueras, Anna, Cesar, Sergi, Arbelo, Elena, Jordà, Paloma, García-Álvarez, Ana, Cruzalegui, Jose Carlos, Merchan, Erika Fernanda, Fiol, Victoria, Brugada, Josep, Brugada, Ramon, Campuzano, Oscar
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Frontiers Media S.A. 2021
Konular:
Pediatrics
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC7938306/
https://ncbi.nlm.nih.gov/pubmed/33692971
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fped.2020.601708
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