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KIF4 regulates neuronal morphology and seizure susceptibility via the PARP1 signaling pathway

Epilepsy is a common neurological disease worldwide, and one of its causes is genetic abnormalities. Here, we identified a point mutation in KIF4A, a member of kinesin superfamily molecular motors, in patients with neurological disorders such as epilepsy, developmental delay, and intellectual disabi...

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Detalles Bibliográficos
Autores principales:	Wan, Yuansong, Morikawa, Momo, Morikawa, Manatsu, Iwata, Suguru, Naseer, Muhammad Imran, Ahmed Chaudhary, Adeel Gulzar, Tanaka, Yosuke, Hirokawa, Nobutaka
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Rockefeller University Press 2022
Materias:	Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9735414/ https://www.ncbi.nlm.nih.gov/pubmed/36482480 http://dx.doi.org/10.1083/jcb.202208108

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