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Human iPS cell model of type 3 long QT syndrome recapitulates drug-based phenotype correction
Long QT syndrome is a potentially life-threatening disease characterized by delayed repolarization of cardiomyocytes, QT interval prolongation in the electrocardiogram, and a high risk for sudden cardiac death caused by ventricular arrhythmia. The genetic type 3 of this syndrome (LQT3) is caused by...
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| Publicado no: | Basic Res Cardiol |
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| Main Authors: | , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Springer Berlin Heidelberg
2016
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4724360/ https://ncbi.nlm.nih.gov/pubmed/26803770 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00395-016-0530-0 |
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