Cargando…
Commentary: Next Generation Sequencing and Linkage Analysis for the Molecular Diagnosis of a Novel Overlapping Syndrome Characterized by Hypertrophic Cardiomyopathy and Typical Electrical Instability of Brugada Syndrome
Autores principales: | Monasky, Michelle M., Ciconte, Giuseppe, Anastasia, Luigi, Pappone, Carlo |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5733025/ https://www.ncbi.nlm.nih.gov/pubmed/29311983 http://dx.doi.org/10.3389/fphys.2017.01056 |
Ejemplares similares
-
Right ventricular electromechanical abnormalities in Brugada syndrome: is this a cardiomyopathy?
por: Pappone, Carlo, et al.
Publicado: (2020) -
Brugada Syndrome: Oligogenic or Mendelian Disease?
por: Monasky, Michelle M., et al.
Publicado: (2020) -
Brugada Syndrome: Warning of a Systemic Condition?
por: D'Imperio, Sara, et al.
Publicado: (2021) -
Common modulators of Brugada syndrome phenotype do not affect SCN5A prognostic value
por: Pappone, Carlo, et al.
Publicado: (2021) -
Calcium in Brugada Syndrome: Questions for Future Research
por: Monasky, Michelle M., et al.
Publicado: (2018)