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. 2020 Aug 10;22(12):2060–2070. doi: 10.1038/s41436-020-0923-1

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© The Author(s) 2020

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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.

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Fig. 4 — Phenotypic features associate with discrete genetic etiologies at specific time points when binned into 3-month intervals. Clinical terms associated with individual genes occur at different time intervals. The Human Phenotype Ontology (HPO) terms associated with (a) SCN1A, (b) STXBP1, (c) SCN2A, and (d) KCNQ2 are shown as an example with only the time interval with the most significant association for each HPO term shown. X-axis denotes patient age, y-axis denotes −log₁₀ of the p value (Fisher’s exact test). EEG electroencephalogram.