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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Bibliographische Detailangaben
Hauptverfasser: Petrecca, Kevin, Atanasiu, Roxana, Akhavan, Armin, Shrier, Alvin
Format: Artigo
Sprache:Inglês
Veröffentlicht: Blackwell Science Inc 1999
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Original Articles
Online Zugang: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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