Clinical and genetic features of Australian families with long QT syndrome: A registry-based study

BACKGROUND: Familial long QT syndrome (LQTS) is a primary arrhythmogenic disorder caused by mutations in ion channel genes. The phenotype ranges from asymptomatic individuals to sudden cardiac arrest and death. LQTS is a rare but significant health problem for which global data should exist. This st...

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Detalles Bibliográficos
Autores principales: Burns, Charlotte, Ingles, Jodie, Davis, Andrew M., Connell, Vanessa, Gray, Belinda, Hunt, Lauren, McGaughran, Julie, Semsarian, Christopher
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2016
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5129121/
https://www.ncbi.nlm.nih.gov/pubmed/27920829
http://dx.doi.org/10.1016/j.joa.2016.02.001

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5129121/
https://www.ncbi.nlm.nih.gov/pubmed/27920829
http://dx.doi.org/10.1016/j.joa.2016.02.001

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