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SCN1B and SCN2B gene variants analysis in dravet syndrome patients: Analysis of 22 cases

Previous research identified SCN1B variants in some cases of Dravet syndrome (DS). We investigated whether SCN1B and SCN2B variants are commonly happened in DS patients without SCN1A variants. A total of 22 DS patients without SCN1A variants and 100 healthy controls were enrolled in this genetic stu...

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Detalles Bibliográficos
Autores principales:	Gong, Jiao-E., Liao, Hong-Mei, Long, Hong-Yu, Li, Xiang-Min, Long, Li-Li, Zhou, Luo, Gu, Wen-Ping, Lu, Shao-Hua, Qu, Qiang, Yang, Li-Min, Xiao, Bo, Qu, Jian
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Wolters Kluwer Health 2019
Materias:	Research Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6455785/ https://www.ncbi.nlm.nih.gov/pubmed/30921204 http://dx.doi.org/10.1097/MD.0000000000014974

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