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L51P, a novel mutation in the PAS domain of hERG channel, confers long QT syndrome by impairing channel activation
The human ether-à-go-go-related gene (hERG) potassium channel mediates the repolarization of ventricular action potentials. Mutations in the KCNH2 cause long QT syndrome (LQTS) and are associated with cardiac arrhythmias and sudden death. Here, we functionally analyzed a mutation of hERG potassium c...
Gorde:
| Argitaratua izan da: | Am J Transl Res |
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| Egile Nagusiak: | , , , , , , |
| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
e-Century Publishing Corporation
2020
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| Gaiak: | |
| Sarrera elektronikoa: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7791479/ https://ncbi.nlm.nih.gov/pubmed/33437379 |
| Etiketak: |
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