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Upgraded molecular models of the human KCNQ1 potassium channel
The voltage-gated potassium channel KCNQ1 (K(V)7.1) assembles with the KCNE1 accessory protein to generate the slow delayed rectifier current, I(KS), which is critical for membrane repolarization as part of the cardiac action potential. Loss-of-function (LOF) mutations in KCNQ1 are the most common c...
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| Publicado en: | PLoS One |
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| Autores principales: | , , , , , , , , |
| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
Public Library of Science
2019
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| Materias: | |
| Acceso en línea: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6743773/ https://ncbi.nlm.nih.gov/pubmed/31518351 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0220415 |
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