Different experiences of two PRRT2-associated self-limited familial infantile epilepsy

To analyze the clinical characteristics and PRRT2 gene mutation of self-limited familial infantile epilepsy and evaluate the treatment responses of different antiepileptic drugs in self-limited familial infantile epilepsy. We reviewed the clinical feature and genetic mutation results and treatment r...

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Detalles Bibliográficos
Autores principales: Zhao, Qianlei, Liu, Zhenwei, Hu, Ying, Fang, Shiyu, Zheng, Feixia, Li, Xiucui, Li, Feng, Lin, Zhongdong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2020
Materias:
Evidence- and experienced-based Neurology article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7383030/
https://www.ncbi.nlm.nih.gov/pubmed/32246320
http://dx.doi.org/10.1007/s13760-020-01348-9

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7383030/
https://www.ncbi.nlm.nih.gov/pubmed/32246320
http://dx.doi.org/10.1007/s13760-020-01348-9

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