A Rare KIF1A Missense Mutation Enhances Synaptic Function and Increases Seizure Activity

Although genetic factors are considered a main etiology of epilepsy, the causes of genetic epilepsy in the majority of epilepsy patients remain unknown. Kinesin family member 1A (KIF1A), a neuron-specific motor protein that moves along with microtubules, is responsible for the transport of membranou...

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Detalles Bibliográficos
Autores principales: Guo, Yi, Chen, Yuanyuan, Yang, Min, Xu, Xin, Lin, Zijun, Ma, Junhong, Chen, Hongnian, Hu, Yida, Ma, Yuanlin, Wang, Xuefeng, Tian, Xin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7056823/
https://www.ncbi.nlm.nih.gov/pubmed/32174959
http://dx.doi.org/10.3389/fgene.2020.00061

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7056823/
https://www.ncbi.nlm.nih.gov/pubmed/32174959
http://dx.doi.org/10.3389/fgene.2020.00061

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