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KCNE2 confers background current characteristics to the cardiac KCNQ1 potassium channel
Mutations in HERG and KCNQ1 (or KVLQT1) genes cause the life-threatening Long QT syndrome. These genes encode K(+) channel pore-forming subunits that associate with ancillary subunits from the KCNE family to underlie the two components, I(Kr) and I(Ks), of the human cardiac delayed rectifier current...
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| Main Authors: | , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Oxford University Press
2000
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC305874/ https://ncbi.nlm.nih.gov/pubmed/11101505 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/emboj/19.23.6326 |
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