Risk of Syncope in Family Members Who Are Genotype Negative for a Family-Associated Long QT Syndrome Mutation

BACKGROUND: Current clinical diagnosis of long-QT syndrome (LQTS) includes genetic testing of family members of mutation positive patients. The present study was designed to assess the clinical course of individuals who are found negative for the LQTS-causing mutation in their families. METHODS AND...

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Detalhes bibliográficos
Main Authors: Barsheshet, Alon, Moss, Arthur J., McNitt, Scott, Polonsky, Slava, Lopes, Coeli M., Zareba, Wojciech, Robinson, Jennifer L., Ackerman, Michael J., Benhorin, Jesaia, Kaufman, Elizabeth S., Towbin, Jeffrey A., Vincent, G. Michael, Qi, Ming, Goldenberg, Ilan
Formato: Artigo
Idioma:Inglês
Publicado em: 2011
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3690290/
https://ncbi.nlm.nih.gov/pubmed/21831960
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1161/CIRCGENETICS.111.960179
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