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...
Kaydedildi:
| Yayımlandı: | EMBO J |
|---|---|
| Asıl Yazarlar: | , , , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Nature Publishing Group
2000
|
| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC305874/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/11101505/ https://ncbi.nlm.nih.govhttps://doi.org/10.1093/emboj/19.23.6326 |
| Etiketler: |
Etiket eklenmemiş, İlk siz ekleyin!
|