A novel mutation in the sodium channel α1 subunit gene in a child with Dravet syndrome in Turkey☆

Dravet syndrome is a rare epileptic encephalopathy characterized by frequent seizures beginning in the first year of life and behavioral disorders. Mutations in the sodium channel α1 subunit gene are the main cause of this disease. We report two patients with refractory seizures and psychomotor reta...

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Detalles Bibliográficos
Autores principales: Arslan, Mutluay, Yiş, Uluç, Çağlayan, Hande, Akin, Rıdvan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2013
Materias:
Research and Report Article: Neuroimaging and Neural Regeneration
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4145926/
https://www.ncbi.nlm.nih.gov/pubmed/25206388
http://dx.doi.org/10.3969/j.issn.1673-5374.2013.10.011

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4145926/
https://www.ncbi.nlm.nih.gov/pubmed/25206388
http://dx.doi.org/10.3969/j.issn.1673-5374.2013.10.011

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