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Trehalose Treatment in Zebrafish Model of Lafora Disease

Mutations in the EPM2A gene encoding laforin cause Lafora disease (LD), a progressive myoclonic epilepsy characterized by drug-resistant seizures and progressive neurological impairment. To date, rodents are the only available models for studying LD; however, their use for drug screening is limited...

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Detalles Bibliográficos
Autores principales:	Della Vecchia, Stefania, Ogi, Asahi, Licitra, Rosario, Abramo, Francesca, Nardi, Gabriele, Mero, Serena, Landi, Silvia, Battini, Roberta, Sicca, Federico, Ratto, Gian Michele, Santorelli, Filippo Maria, Marchese, Maria
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	MDPI 2022
Materias:	Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9224929/ https://www.ncbi.nlm.nih.gov/pubmed/35743315 http://dx.doi.org/10.3390/ijms23126874

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