In silico investigation of the short QT syndrome, using human ventricle models incorporating electromechanical coupling

Introduction: Genetic forms of the Short QT Syndrome (SQTS) arise due to cardiac ion channel mutations leading to accelerated ventricular repolarization, arrhythmias and sudden cardiac death. Results from experimental and simulation studies suggest that changes to refractoriness and tissue vulnerabi...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Hauptverfasser: Adeniran, Ismail, Hancox, Jules C., Zhang, Henggui
Format: Artigo
Sprache:Inglês
Veröffentlicht: Frontiers Media S.A. 2013
Schlagworte:
Physiology
Online Zugang:https://ncbi.nlm.nih.gov/pmc/articles/PMC3701879/
https://ncbi.nlm.nih.gov/pubmed/23847545
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fphys.2013.00166
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!

Ähnliche Einträge