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PRRT2 controls neuronal excitability by negatively modulating Na(+) channel 1.2/1.6 activity

See Lerche (doi:10.1093/brain/awy073) for a scientific commentary on this article. Proline-rich transmembrane protein 2 (PRRT2) is the causative gene for a heterogeneous group of familial paroxysmal neurological disorders that include seizures with onset in the first year of life (benign familial in...

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Dades bibliogràfiques
Publicat a:Brain
Autors principals: Fruscione, Floriana, Valente, Pierluigi, Sterlini, Bruno, Romei, Alessandra, Baldassari, Simona, Fadda, Manuela, Prestigio, Cosimo, Giansante, Giorgia, Sartorelli, Jacopo, Rossi, Pia, Rubio, Alicia, Gambardella, Antonio, Nieus, Thierry, Broccoli, Vania, Fassio, Anna, Baldelli, Pietro, Corradi, Anna, Zara, Federico, Benfenati, Fabio
Format: Artigo
Idioma:Inglês
Publicat: Oxford University Press 2018
Matèries:
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC5888929/
https://ncbi.nlm.nih.gov/pubmed/29554219
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/brain/awy051
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