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High-throughput functional mapping of variants in an arrhythmia gene, KCNE1, reveals novel biology
BACKGROUND: KCNE1 encodes a 129-residue cardiac potassium channel (I(Ks)) subunit. KCNE1 variants are associated with long QT syndrome and atrial fibrillation. However, most variants have insufficient evidence of clinical consequences and thus limited clinical utility. RESULTS: Here, we demonstrate...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10168370/ https://www.ncbi.nlm.nih.gov/pubmed/37162834 http://dx.doi.org/10.1101/2023.04.28.538612 |