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Novel SZT2 mutations in three patients with developmental and epileptic encephalopathies

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The seizure threshold 2 (SZT2) gene encodes a large, highly conserved protein that lowers seizure threshold and may also enhance epileptogenesis. In this study, three patients diagnosed with SZT2‐related developmental… Click to show full abstract

The seizure threshold 2 (SZT2) gene encodes a large, highly conserved protein that lowers seizure threshold and may also enhance epileptogenesis. In this study, three patients diagnosed with SZT2‐related developmental and epileptic encephalopathies (DEEs) were reviewed aiming to expand knowledge of the genotype and phenotype of SZT2 mutations.

Keywords: novel szt2; epileptic encephalopathies; mutations three; szt2 mutations; three patients; developmental epileptic

Journal Title: Molecular Genetics & Genomic Medicine
Year Published: 2019

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