N-linked glycosylation sites determine HERG channel surface membrane expression

1. Long QT syndrome (LQT) is an electrophysiological disorder that can lead to sudden death from cardiac arrhythmias. One form of LQT has been attributed to mutations in the human ether-a-go-go-related gene (HERG) that encodes a voltage-gated cardiac K(+) channel. While a recent report indicates tha...

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Detalles Bibliográficos
Main Authors: Petrecca, Kevin, Atanasiu, Roxana, Akhavan, Armin, Shrier, Alvin
Formato: Artigo
Idioma:Inglês
Publicado: Blackwell Science Inc 1999
Assuntos:
Original Articles
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC2269130/
https://ncbi.nlm.nih.gov/pubmed/9925876
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/j.1469-7793.1999.041ad.x
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