Large-scale structural alteration of brain in epileptic children with SCN1A mutation

OBJECTIVE: Mutations in SCN1A gene encoding the alpha 1 subunit of the voltage gated sodium channel are associated with several epilepsy syndromes including genetic epilepsy with febrile seizures plus (GEFS +) and severe myoclonic epilepsy of infancy (SMEI). However, in most patients with SCN1A muta...

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Detalles Bibliográficos
Autores principales: Lee, Yun-Jeong, Yum, Mi-Sun, Kim, Min-Jee, Shim, Woo-Hyun, Yoon, Hee Mang, Yoo, Il Han, Lee, Jiwon, Lim, Byung Chan, Kim, Ki Joong, Ko, Tae-Sung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2017
Materias:
Regular Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5479971/
https://www.ncbi.nlm.nih.gov/pubmed/28664031
http://dx.doi.org/10.1016/j.nicl.2017.06.002

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5479971/
https://www.ncbi.nlm.nih.gov/pubmed/28664031
http://dx.doi.org/10.1016/j.nicl.2017.06.002

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