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. 2023 Apr 15;14:2157. doi: 10.1038/s41467-023-37928-5

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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 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. 8 — A core gene set associated with the severity of HSCR was identified. Additional alternations in genes implicated in RNA splicing and oxidative phosphorylation (OXPHOS) were found in L-HSCR cases. High HDAC1 activity is associated with defective neuronal differentiation, as observed in HSCR-ENCCs. Only the representative genes/pathways are shown.