Cargando…
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...
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: | |
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 |
Ejemplares similares
-
Evaluating a custom-designed aid to improve communication of genetic results in families with hypertrophic cardiomyopathy: study protocol for a randomised controlled trial
por: Burns, Charlotte, et al.
Publicado: (2019) -
The Australian Genetic Heart Disease Registry: Protocol for a Data Linkage Study
por: Butters, Alexandra, et al.
Publicado: (2023) -
Development of a communication aid for explaining hypertrophic cardiomyopathy genetic test results
por: Smagarinsky, Yana, et al.
Publicado: (2017) -
Molecular autopsy in victims of inherited arrhythmias
por: Semsarian, Christopher, et al.
Publicado: (2016) -
Relations between right ventricular morphology and clinical, electrical and genetic parameters in Brugada Syndrome
por: Gray, Belinda, et al.
Publicado: (2018)