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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...

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Detalles Bibliográficos
Autores principales: Landolfi, Annamaria, Barone, Paolo, Erro, Roberto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
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