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...

Popoln opis

Bibliografske podrobnosti

izdano v:	EMBO J
Principais autores:	Tinel, Norbert, Diochot, Sylvie, Borsotto, Marc, Lazdunski, Michel, Barhanin, Jacques
Format:	Artigo
Jezik:	Inglês
Izdano:	Nature Publishing Group 2000
Teme:	Articles
Online dostop:	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
Oznake:	Označite Brez oznak, prvi označite!