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. 2023 Jul 20;31(7-8):263–271. doi: 10.1007/s12471-023-01799-8

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© The Author(s) 2023

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.

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Fig. 2 — SCN5A-1795insD founder population a Pedigree, with circles indicating SCN5A-1795insD carriers suffering sudden cardiac death (SCD), ventricular fibrillation (VF) and/or ventricular tachycardia (VT). PM pacemaker, HYP hypertension. b Scatterplots showing overlap between mutation carriers (filled boxes) and non-carriers (open circles) for PQ interval versus QRS duration, ST-segment elevation versus heart rate-corrected QT interval (QTc) and QTc versus RR interval. a was reprinted from: Rivaud et al. [7]. b was reprinted under a CC-BY licence from: Postema et al. [3]