Molecular Approach of Hereditary Arrhythmias, Long QT Syndrome, and Arrhythmogenic Right Ventricular Cardiomyopathy

BACKGROUND: Hereditary cardiac arrhythmias result from mutations in various genes encoding ion channels. One major channelopathy is long QT syndrome, which has excellent genetic and clinical heterogeneity. Arrhythmogenic right ventricular cardiomyopathy, another hereditary arrhythmia type, also show...

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Detalles Bibliográficos
Autores principales: Saat, Hanife, Şahin, İbrahim, Bağış Erdem, Haktan, Özgür, Senem, Terlemez Tokgöz, Semiha, Bahsi, Taha
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Turkish Society of Cardiology 2022
Materias:
Original Investigation
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9361120/
https://www.ncbi.nlm.nih.gov/pubmed/35703482
http://dx.doi.org/10.5152/AnatolJCardiol.2022.1324

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9361120/
https://www.ncbi.nlm.nih.gov/pubmed/35703482
http://dx.doi.org/10.5152/AnatolJCardiol.2022.1324

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