IndraLab

Statements


KCN binds KCNE1 and KCNQ1. 2 / 2
| 2

sparser
"KvLQT1 and minK associate to form the functional slowly activated delayed rectifier potassium channel ( I Ks ) [12,13] while HERG and MiRP1 associate to form the rapidl[MISSING/INVALID CREDENTIALS: limited to 200 char for Elsevier]"

sparser
"Genetic defect is located in the KCNQ1 and KCNE1 (LQT1) genes that form the slow component of the delayed rectifier potassium channel complex (90 and 10% of cases, resp.)."