A novel LGI1 mutation causing autosomal dominant lateral temporal lobe epilepsy confirmed by a precise knock‐in mouse model

AIMS: This study aimed to explore the pathomechanism of a mutation on the leucine‐rich glioma inactivated 1 gene (LGI1) identified in a family having autosomal dominant lateral temporal lobe epilepsy (ADLTE), using a precise knock‐in mouse model. METHODS AND RESULTS: A novel LGI1 mutation, c.152A>...

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Detalles Bibliográficos
Autores principales: Hu, Ping, Wu, Dan, Zang, Yan‐Yu, Wang, Yan, Zhou, Ya‐Ping, Qiao, Fengchang, Teng, Xiao‐Yu, Chen, Jiang, Li, Qing‐Qing, Sun, Jia‐Hui, Liu, TingTing, Feng, Hao‐Yang, Zhou, Qi‐Gang, Shi, Yun Stone, Xu, Zhengfeng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8739050/
https://www.ncbi.nlm.nih.gov/pubmed/34767694
http://dx.doi.org/10.1111/cns.13761

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8739050/
https://www.ncbi.nlm.nih.gov/pubmed/34767694
http://dx.doi.org/10.1111/cns.13761

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