Screening for Rare Coding Variants That Associate With the QTc Interval in Iceland

BACKGROUND: Long‐QT syndrome (LQTS) is a cardiac repolarization abnormality that can lead to sudden cardiac death. The most common causes are rare coding variants in the genes KCNQ1, KCNH2, and SCN5A. The data on LQTS epidemiology are limited, and information on expressivity and penetrance of pathog...

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Detalles Bibliográficos
Autores principales: Sveinbjornsson, Gardar, Benediktsdottir, Bara D., Sigfusson, Gunnlaugur, Norland, Kristjan, Davidsson, Olafur B., Thorolfsdottir, Rosa B., Tragante, Vinicius, Arnadottir, Gudny A., Jensson, Brynjar O., Katrinardottir, Hildigunnur, Fridriksdottir, Run, Gudmundsdottir, Hallbera, Aegisdottir, Hildur M., Fridriksson, Brynjar, Thorgeirsson, Gudmundur, Magnusson, Vidar, Oddsson, Asmundur, Sulem, Patrick, Gudbjartsson, Daniel F., Holm, Hilma, Arnar, David O., Stefansson, Kari
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Original Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10382112/
https://www.ncbi.nlm.nih.gov/pubmed/37449562
http://dx.doi.org/10.1161/JAHA.123.029845

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10382112/
https://www.ncbi.nlm.nih.gov/pubmed/37449562
http://dx.doi.org/10.1161/JAHA.123.029845

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