Morphometry and network-based atrophy patterns in SCN1A-related Dravet syndrome

Mutations of the voltage-gated sodium channel SCN1A gene (MIM#182389) are among the most clinically relevant epilepsy-related genetic mutations and present variable phenotypes, from the milder genetic epilepsy with febrile seizures plus to Dravet syndrome, a severe developmental and epileptic enceph...

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Detalles Bibliográficos
Autores principales: Lenge, Matteo, Balestrini, Simona, Mei, Davide, Macconi, Letizia, Caligiuri, Maria Eugenia, Cuccarini, Valeria, Aquino, Domenico, Mazzi, Federica, d’Incerti, Ludovico, Darra, Francesca, Bernardina, Bernardo Dalla, Guerrini, Renzo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10431750/
https://www.ncbi.nlm.nih.gov/pubmed/37344172
http://dx.doi.org/10.1093/cercor/bhad224

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10431750/
https://www.ncbi.nlm.nih.gov/pubmed/37344172
http://dx.doi.org/10.1093/cercor/bhad224

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