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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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Bibliografski detalji
Glavni autori: 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
Format: Artigo
Jezik:Inglês
Izdano: 2011
Teme:
Online pristup: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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