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Article

SCN2A and Its Related Epileptic Phenotypes

2021-03-27

Abstract excerpt

Abstract Epilepsies due to SCN2A mutations can present with a broad range of phenotypes that are still not fully understood. Clinical characteristics of SNC2A-related epilepsy may vary from neonatal benign epilepsy to early-onset epileptic encephalopathy, including Ohtahara syndrome and West syndrome, and epileptic encephalopathies occurring at later ages (usually within the first 10 years of life). Some patient m...

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Literature Corpus work
42acbe23-f2aa-526e-bfa7-a28e2c797ea2
DOI
10.1055/s-0041-1727097
Open publication

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SCN2A and Its Related Epileptic PhenotypesDOI 10.1055/s-0041-1727097
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