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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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| Publicado no: | Brain |
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| Main Authors: | , , , , , , , , , , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Oxford University Press
2018
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| Assuntos: | |
| Acesso em linha: | 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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