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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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| 主要な著者: | , , , |
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| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Blackwell Science Inc
1999
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| 主題: | |
| オンライン･アクセス: | 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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