Mutation-specific Risk in Two Genetic Forms of Type-3 Long QT Syndrome

The clinical course of patients with two relatively common LQT3 mutations has not been well described. In this study, we investigated the mutational-specific risk in patients with deletional (ΔKPQ) and missense (D1790G) mutations involving the SCN5A gene. The study population involved 50 patients wi...

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Главные авторы: Liu, Judy F., Moss, Arthur J., Jons, Christian, Benhorin, Jesaia, Schwartz, Peter J., Spazzolini, Carla, Crotti, Lia, Ackerman, Michael J., McNitt, Scott, Robinson, Jennifer L., Qi, Ming, Goldenberg, Ilan, Zareba, Wojciech
Формат: Artigo
Язык:Inglês
Опубликовано: 2010
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Article
Online-ссылка:https://ncbi.nlm.nih.gov/pmc/articles/PMC2813568/
https://ncbi.nlm.nih.gov/pubmed/20102920
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.amjcard.2009.08.676
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