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The Spectrum of PRRT2-Associated Disorders: Update on Clinical Features and Pathophysiology
Mutations in the PRRT2 (proline-rich transmembrane protein 2) gene have been identified as the main cause of an expanding spectrum of disorders, including paroxysmal kinesigenic dyskinesia and benign familial infantile epilepsy, which places this gene at the border between epilepsy and movement diso...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Frontiers Media S.A.
2021
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7969989/ https://www.ncbi.nlm.nih.gov/pubmed/33746883 http://dx.doi.org/10.3389/fneur.2021.629747 |