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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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Main Authors: | , , , , , , , , , , |
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Formato: | Artigo |
Idioma: | Inglês |
Publicado em: |
Frontiers Media S.A.
2020-02-01
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Colecção: | Frontiers in Genetics |
Assuntos: | |
Acesso em linha: | https://www.frontiersin.org/article/10.3389/fgene.2020.00061/full |
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