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SYNGAP1 encephalopathyA distinctive generalized developmental and epileptic encephalopathy

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Figure

Figure 1 Schematic presentation of SYNGAP1 mutations and microdeletions (A) in patients of our cohort or (B) previously published in the literature
Table 1 Phenotypes in patients with SYNGAP1 mutations and microdeletions
Table 1 Phenotypes in patients with SYNGAP1 mutations and microdeletions (continued)
Figure 2 Ictal EEG registration during eyelid myoclonia–myoclonic–atonic seizure
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