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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

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