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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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| Main Authors: | , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Blackwell Science Inc
1999
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| Assuntos: | |
| Acesso em linha: | 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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