Loading...
A recessive C-terminal Jervell and Lange-Nielsen mutation of the KCNQ1 channel impairs subunit assembly
The LQT1 locus (KCNQ1) has been correlated with the most common form of inherited long QT (LQT) syndrome. LQT patients suffer from syncopal episodes and high risk of sudden death. The KCNQ1 gene encodes K(v)LQT1 α–subunits, which together with auxiliary IsK (KCNE1, minK) subunits form IK(s) K(+) cha...
Na minha lista:
| Udgivet i: | EMBO J |
|---|---|
| Main Authors: | , , , , , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
Nature Publishing Group
2000
|
| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC305570/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/10654932/ https://ncbi.nlm.nih.govhttps://doi.org/10.1093/emboj/19.3.332 |
| Tags: |
Tilføj Tag
Ingen Tags, Vær først til at tagge denne postø!
|