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. 2018 Aug 16;25(9):2047–2057. doi: 10.1038/s41380-018-0210-6

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© The Author(s) 2018

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. 1 — Segregation analysis for rs151326868 (chr9:99404124G>C; AAED1gene) and the SNV at chr8:124346225T>C (ATAD2gene) in family P2. ADHD-affected individuals are depicted by black symbols, unaffected family members are shown by white symbols and individuals with unknown ADHD status are represented by a question mark in the symbol. An asterisk beneath an individual indicates that DNA was used for whole-exome sequencing analysis. Non-reference alleles are depicted in bold.