Characterization of human cardiac Na+ channel mutations in the congenital long QT syndrome
Author:
Publisher
Proceedings of the National Academy of Sciences
Subject
Multidisciplinary
Reference32 articles.
1. The long Q-T syndrome
2. Evidence of genetic heterogeneity in Romano-Ward long QT syndrome. Analysis of 23 families.
3. A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome
4. SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome
5. Primary structure and functional expression of the human cardiac tetrodotoxin-insensitive voltage-dependent sodium channel.
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