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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Detalhes bibliográficos
Main Authors: 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
Formato: Artigo
Idioma:Inglês
Publicado em: 2010
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Article
Acesso em linha: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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