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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...
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 |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2023
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Materias: | |
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 |
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