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Cardiac Subtype-Specific Modeling of K(v)1.5 Ion Channel Deficiency Using Human Pluripotent Stem Cells
The ultrarapid delayed rectifier K(+) current (I(Kur)), mediated by K(v)1.5 channels, constitutes a key component of the atrial action potential. Functional mutations in the underlying KCNA5 gene have been shown to cause hereditary forms of atrial fibrillation (AF). Here, we combine targeted genetic...
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| Publicat a: | Front Physiol |
|---|---|
| Autors principals: | , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Frontiers Media S.A.
2017
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5498524/ https://ncbi.nlm.nih.gov/pubmed/28729840 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fphys.2017.00469 |
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