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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Hlavní autoři: 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
Médium: Artigo
Jazyk:Inglês
Vydáno: 2011
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Article
On-line přístup: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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