Associated Papers
High-throughput functional mapping of variants in an arrhythmia gene, KCNE1, reveals novel biology.
Muhammad A et al.
Genome Medicine, 2024
38816749 (PubMed )
Supplement: 13073_2024_1340_MOESM2_ESM.xlsx › LitReview
New mutations in the KVLQT1 potassium channel that cause long-QT syndrome.
Li H et al.
Circulation, 1998
Diseases caused by voltage-gated ion channels.
Fontaine B et al.
Molecular Aspects of Medicine, 1997
Molecular genetics of long QT syndrome from genes to patients.
Wang Q et al.
Current Opinion in Cardiology, 1997
Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias.
Wang Q et al.
Nature Genetics, 1996
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