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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...

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Bibliografiske detaljer
Udgivet i:EMBO J
Main Authors: Schmitt, Nicole, Schwarz, Martin, Peretz, Asher, Abitbol, Ilane, Attali, Bernard, Pongs, Olaf
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
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