SCN1A Gene Mutation and Adaptive Functioning in 18 Vietnamese Children with Dravet Syndrome

BACKGROUND AND PURPOSE: Dravet syndrome is a rare and severe type of epilepsy in infants. The heterogeneity in the overall intellectual disability that these patients suffer from has been attributed to differences in genetic background and epilepsy severity. METHODS: Eighteen Vietnamese children dia...

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Detalles Bibliográficos
Autores principales: Do, Thi Thu Hang, Vu, Diem My, Huynh, Thi Thuy Kieu, Le, Thi Khanh Van, Sohn, Eun-Hwa, Le, Thieu Mai Thao, Ha, Huu Hao, Bui, Chi Bao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Neurological Association 2017
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5242153/
https://www.ncbi.nlm.nih.gov/pubmed/28079314
http://dx.doi.org/10.3988/jcn.2017.13.1.62

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5242153/
https://www.ncbi.nlm.nih.gov/pubmed/28079314
http://dx.doi.org/10.3988/jcn.2017.13.1.62

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