Treating seizures in SYN1-related epilepsy: a systematic review

The synapsin 1 gene (SYN1), located on chromosome X (Xp11.23), encodes for a neuronal phosphoprotein, implicated in different aspects of presynaptic physiology [1]. The SYN1 gene is composed of 13 exons, encoding for two protein isoforms (of 669 and 705 amino acids), resulting from alternative splicing [2].

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