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. 2022 Jan 18;12:902. doi: 10.1038/s41598-021-04723-5

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© The Author(s) 2022

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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(a) Pedigree of the family with the SHANK3 missense variant c.808C>A, p.L270M. ± denotes presence/absence of the variant. (b + c) Domain structure of Shank3 and 3D-structure of the Shank3 N-terminus (model based on the crystal structure of the Shank3 N-terminus (5G4X)¹⁸. The positions of the N-terminal missense mutations examined in this study are indicated.