An Emerging Role of PRRT2 in Regulating Growth Cone Morphology

Mutations in the PRRT2 gene are the main cause for a group of paroxysmal neurological diseases including paroxysmal kinesigenic dyskinesia, episodic ataxia, benign familial infantile seizures, and hemiplegic migraine. In the mature central nervous system, the protein has both a functional and a stru...

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Detalles Bibliográficos
Autores principales: Savino, Elisa, Guarnieri, Fabrizia Claudia, Tsai, Jin-Wu, Corradi, Anna, Benfenati, Fabio, Valtorta, Flavia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8534124/
https://www.ncbi.nlm.nih.gov/pubmed/34685646
http://dx.doi.org/10.3390/cells10102666

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8534124/
https://www.ncbi.nlm.nih.gov/pubmed/34685646
http://dx.doi.org/10.3390/cells10102666

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