Structural and Functional Brain Abnormalities in Mouse Models of Lafora Disease

Mutations in the EPM2A and EPM2B genes, encoding laforin and malin proteins respectively, are responsible for Lafora disease, a fatal form of progressive myoclonus epilepsy with autosomal recessive inheritance. Neuroimaging studies of patients with Lafora disease have shown different degrees of brai...

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Detalles Bibliográficos
Autores principales: Burgos, Daniel F., Cussó, Lorena, Sánchez-Elexpuru, Gentzane, Calle, Daniel, Perpinyà, Max Bautista, Desco, Manuel, Serratosa, José M., Sánchez, Marina P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7589150/
https://www.ncbi.nlm.nih.gov/pubmed/33092303
http://dx.doi.org/10.3390/ijms21207771

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7589150/
https://www.ncbi.nlm.nih.gov/pubmed/33092303
http://dx.doi.org/10.3390/ijms21207771

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