Proline-rich transmembrane protein 2 (PRRT2) regulates the actin cytoskeleton during synaptogenesis

Mutations in proline-rich transmembrane protein 2 (PRRT2) have been recently identified as the leading cause of a clinically heterogeneous group of neurological disorders sharing a paroxysmal nature, including paroxysmal kinesigenic dyskinesia and benign familial infantile seizures. To date, studies...

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Detalles Bibliográficos
Autores principales: Savino, Elisa, Cervigni, Romina Inès, Povolo, Miriana, Stefanetti, Alessandra, Ferrante, Daniele, Valente, Pierluigi, Corradi, Anna, Benfenati, Fabio, Guarnieri, Fabrizia Claudia, Valtorta, Flavia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7560900/
https://www.ncbi.nlm.nih.gov/pubmed/33056987
http://dx.doi.org/10.1038/s41419-020-03073-w

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7560900/
https://www.ncbi.nlm.nih.gov/pubmed/33056987
http://dx.doi.org/10.1038/s41419-020-03073-w

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