A novel SCN8A variant of unknown significance in pediatric epilepsy: a case report

Variants in SCN8A are associated with several diseases, including developmental and epileptic encephalopathy, intermediate epilepsy or mild-to-moderate developmental and epileptic encephalopathy, self-limited familial infantile epilepsy, neurodevelopmental delays with generalized epilepsy, neurodeve...

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Detalles Bibliográficos
Autores principales: Bouzroud, Wafaa, Tazzite, Amal, Boussakri, Ikhlass, Gazzaz, Bouchaïb, Dehbi, Hind
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2023
Materias:
Case Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10387795/
https://www.ncbi.nlm.nih.gov/pubmed/37498161
http://dx.doi.org/10.1177/03000605231187931

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10387795/
https://www.ncbi.nlm.nih.gov/pubmed/37498161
http://dx.doi.org/10.1177/03000605231187931

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