Developmental and epileptic encephalopathy due to SZT2 genomic variants: Emerging features of a syndromic condition-Reference-Cited by-同舟云学术

Developmental and epileptic encephalopathy due to SZT2 genomic variants: Emerging features of a syndromic condition

Published:2020-07 Issue: Volume:108 Page:107097
ISSN:1525-5050
Container-title:Epilepsy & Behavior
language:en
Short-container-title:Epilepsy & Behavior

Author:

Trivisano Marina,Rivera Manuel,Terracciano Alessandra,Ciolfi Andrea,Napolitano Antonio,Pepi Chiara,Calabrese Costanza,Digilio Maria Cristina,Tartaglia Marco,Curatolo Paolo,Vigevano Federico,Specchio Nicola

Publisher

Elsevier BV

Subject

Behavioral Neuroscience,Neurology (clinical),Neurology

Reference29 articles.

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4. Biallelic SZT2 mutations cause infantile encephalopathy with epilepsy and dysmorphic corpus callosum;Basel-Vanagaite;Am J Hum Genet,2013

5. Szt2, a novel gene for seizure threshold in mice;Frankel;Genes Brain Behav,2009

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3. Customized targeted massively parallel sequencing enables the identification of novel pathogenic variants in Tunisian patients with Developmental and Epileptic Encephalopathy;Epilepsia Open;2023-10-23

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