Identification and functional assessment of a <i>KCNH2</i> compound heterozygosity in a patient with presumed idiopathic ventricular fibrillation ascertains the diagnosis of long QT syndrome type 2
- DOI
- 10.1093/europace/euag001
- Published
- 2026-01-09
- Container
- Europace
- Publisher
- Oxford University Press (OUP)
- Open access
- unknown
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Cite this work
BibTeX
@article{allodium:10.1093/europace/euag001,
title = {Identification and functional assessment of a
<i>KCNH2</i>
compound heterozygosity in a patient with presumed idiopathic ventricular fibrillation ascertains the diagnosis of long QT syndrome type 2},
author = {Natálie Janková and Martin Král and Olga Švecová and Jana Zídková and Samuel Lietava and Stanislava Sladeček and Jiří Pacherník and Michal Pásek and Tomáš Novotný and Markéta Bébarová},
year = {2026},
journal = {Europace},
doi = {10.1093/europace/euag001},
url = {https://doi.org/10.1093/europace/euag001}
}RIS
TY - JOUR
TI - Identification and functional assessment of a
<i>KCNH2</i>
compound heterozygosity in a patient with presumed idiopathic ventricular fibrillation ascertains the diagnosis of long QT syndrome type 2
AU - Natálie Janková
AU - Martin Král
AU - Olga Švecová
AU - Jana Zídková
AU - Samuel Lietava
AU - Stanislava Sladeček
AU - Jiří Pacherník
AU - Michal Pásek
AU - Tomáš Novotný
AU - Markéta Bébarová
PY - 2026
JO - Europace
DO - 10.1093/europace/euag001
UR - https://doi.org/10.1093/europace/euag001
ER - APA
Janková, N., Král, M., Švecová, O., Zídková, J., Lietava, S., Sladeček, S., Pacherník, J., Pásek, M., Novotný, T., & Bébarová, M. (2026). Identification and functional assessment of a <i>KCNH2</i> compound heterozygosity in a patient with presumed idiopathic ventricular fibrillation ascertains the diagnosis of long QT syndrome type 2. Europace. https://doi.org/10.1093/europace/euag001
Source records
- crossref · retrieved 2026-09-26T01:55:00.398Z