טוען...
Long QT Syndrome Modelling with Cardiomyocytes Derived from Human-induced Pluripotent Stem Cells
Long QT syndrome (LQTS) is a potentially severe arrhythmogenic disorder, associated with a prolonged QT interval and sudden death, caused by mutations in key genes regulating cardiac electrophysiology. Current strategies to study LQTS in vitro include heterologous systems or animal models. Despite t...
שמור ב:
| הוצא לאור ב: | Arrhythm Electrophysiol Rev |
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| Main Authors: | , , |
| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
Radcliffe Cardiology
2019
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| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6528025/ https://ncbi.nlm.nih.gov/pubmed/31114684 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.15420/aer.2019.1.1 |
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