Variants in BRWD3 associated with X‐linked partial epilepsy without intellectual disability

AIMS: Etiology of the majority patients with idiopathic partial epilepsy (IPE) remains elusive. We thus screened the potential disease‐associated variants in the patients with IPE. METHODS: Trios‐based whole exome sequencing was performed in a cohort of 320 patients with IPE. Frequency and molecular...

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Detalles Bibliográficos
Autores principales: Tian, Mao‐Qiang, Liu, Xiao‐Rong, Lin, Si‐Mei, Wang, Jie, Luo, Sheng, Gao, Liang‐Di, Chen, Xiao‐Bin, Liang, Xiao‐Yu, Liu, Zhi‐Gang, He, Na, Yi, Yong‐Hong, Liao, Wei‐Ping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9873514/
https://www.ncbi.nlm.nih.gov/pubmed/36514184
http://dx.doi.org/10.1111/cns.14057

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9873514/
https://www.ncbi.nlm.nih.gov/pubmed/36514184
http://dx.doi.org/10.1111/cns.14057

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