An interaction between PRRT2 and Na(+)/K(+) ATPase contributes to the control of neuronal excitability

Mutations in PRoline Rich Transmembrane protein 2 (PRRT2) cause pleiotropic syndromes including benign infantile epilepsy, paroxysmal kinesigenic dyskinesia, episodic ataxia, that share the paroxysmal character of the clinical manifestations. PRRT2 is a neuronal protein that plays multiple roles in...

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Bibliographic Details
Published in:Cell Death Dis
Main Authors: Sterlini, Bruno, Romei, Alessandra, Parodi, Chiara, Aprile, Davide, Oneto, Michele, Aperia, Anita, Valente, Pierluigi, Valtorta, Flavia, Fassio, Anna, Baldelli, Pietro, Benfenati, Fabio, Corradi, Anna
Format: Artigo
Language:Inglês
Published: Nature Publishing Group UK 2021
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Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC7969623/
https://ncbi.nlm.nih.gov/pubmed/33731672
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41419-021-03569-z
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