Cargando…
Repeated molecular genetic analysis in Brugada syndrome revealed a novel disease-associated large deletion in the SCN5A gene
Autores principales: | Broendberg, Anders Krogh, Pedersen, Lisbeth Noerum, Nielsen, Jens Cosedis, Jensen, Henrik Kjaerulf |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5419769/ https://www.ncbi.nlm.nih.gov/pubmed/28491684 http://dx.doi.org/10.1016/j.hrcr.2016.02.008 |
Ejemplares similares
-
Ankyrin-2 variants associated with idiopathic ventricular fibrillation storm in patients with intermittent early repolarization pattern
por: Krogh Broendberg, Anders, et al.
Publicado: (2015) -
Targeted next generation sequencing in a young population with suspected inherited malignant cardiac arrhythmias
por: Broendberg, Anders Krogh, et al.
Publicado: (2018) -
Investigating sudden cardiac death – A new paradigm
por: Jensen, Henrik Kjærulf, et al.
Publicado: (2020) -
Outcome after out-of-hospital cardiac arrest in patients with ischaemic and non-ischaemic heart disease: A Danish tertiary-center cohort study
por: Guldfeldt, Marie-Louise Beier, et al.
Publicado: (2022) -
A Novel SCN5A Mutation in a Patient with Coexistence of Brugada Syndrome Traits and Ischaemic Heart Disease
por: Holst, Anders G., et al.
Publicado: (2009)