N‐linked glycosylation sites determine HERG channel surface membrane expression
Author:
Affiliation:
1. Department of Physiology, McGill University, Montréal, Québec, Canada
Publisher
Wiley
Subject
Physiology
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1111/j.1469-7793.1999.041ad.x
Reference26 articles.
1. Coexistence of missense mutation of HERG and mitochondrial DNA in Japanese long QT family;Akimoto K.;Circulation,1996
2. Missense Mutation in the Pore Region of HERG Causes Familial Long QT Syndrome
3. Degradation of proteins within the endoplasmic reticulum
4. A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome
5. A mutation in HERG Associated with Notched T waves in Long QT Syndrome
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