Enhanced sensitivity of laforin- and malin-deficient mice to the convulsant agent pentylenetetrazole

Lafora disease is a rare form of inherited progressive myoclonus epilepsy caused by mutations in the EPM2A gene encoding laforin, or in the EPM2B gene, which encodes malin. It is characterized by the presence of polyglucosan inclusion bodies (Lafora bodies) in brain and other tissues. Genetically en...

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Detalles Bibliográficos
Autores principales: García-Cabrero, Ana M., Sánchez-Elexpuru, Gentzane, Serratosa, José M., Sánchez, Marina P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2014
Materias:
Psychiatry
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4162417/
https://www.ncbi.nlm.nih.gov/pubmed/25309313
http://dx.doi.org/10.3389/fnins.2014.00291

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4162417/
https://www.ncbi.nlm.nih.gov/pubmed/25309313
http://dx.doi.org/10.3389/fnins.2014.00291

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