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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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Detalhes bibliográficos
Main Authors: Schmitt, Nicole, Schwarz, Martin, Peretz, Asher, Abitbol, Ilane, Attali, Bernard, Pongs, Olaf
Formato: Artigo
Idioma:Inglês
Publicado em: Oxford University Press 2000
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC305570/
https://ncbi.nlm.nih.gov/pubmed/10654932
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/emboj/19.3.332
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