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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...
Αποθηκεύτηκε σε:
| Τόπος έκδοσης: | Arrhythm Electrophysiol Rev |
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| Κύριοι συγγραφείς: | , , |
| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
Radcliffe Cardiology
2019
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| Θέματα: | |
| Διαθέσιμο Online: | 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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