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. 2024 Nov 15;14(11):1450. doi: 10.3390/biom14111450

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© 2024 by the authors.

Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).

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Family pedigrees of the described cohort of 21 individuals with CNV in one of the analyzed genes of cardiac channelopathies. From top to bottom: KCNQ1, SCN5A, and RYR2 gene deletion. Phenotypic and genotypic features of probands and their relatives are shown according to the legend on the lower right of the figure. All CNVs are heterozygous unless otherwise specified. JLNS: Jervell and Lange-Nielsen syndrome. HT: hypertrabeculation. LVNC: left ventricular non-compaction. CPVT: catecholaminergic polymorphic ventricular tachycardia.