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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...
Shranjeno v:
| izdano v: | Arrhythm Electrophysiol Rev |
|---|---|
| Main Authors: | , , |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
Radcliffe Cardiology
2019
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| Teme: | |
| Online dostop: | 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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