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. 2021 Dec 2;15:761473. doi: 10.3389/fnins.2021.761473

FIGURE 1.

FIGURE 1

Location of mutation sites of 13 patients in China. Localization of the SYNGAP1 mutations identified in Amino acid positions are based on the longest SynGAP isoform (NM_006772.3). The main phenotype was listed in corresponding domains. *These variations caused truncated proteins.