Cargando...

Astrocytes and neurons produce distinct types of polyglucosan bodies in Lafora Disease

Lafora disease (LD), the most devastating adolescence-onset epilepsy, is caused by mutations in the EPM2A or EPM2B genes, which encode the proteins laforin and malin, respectively. Loss of function of one of these proteins, which are involved in the regulation of glycogen synthesis, induces the accu...

Descrición completa

Gardado en:
Detalles Bibliográficos
Publicado en:Glia
Main Authors: Augé, Elisabet, Pelegrí, Carme, Manich, Gemma, Cabezón, Itsaso, Guinovart, Joan J., Duran, Jordi, Vilaplana, Jordi
Formato: Artigo
Idioma:Inglês
Publicado: 2018
Assuntos:
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC6240358/
https://ncbi.nlm.nih.gov/pubmed/30152044
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/glia.23463
Tags: Engadir etiqueta
Sen Etiquetas, Sexa o primeiro en etiquetar este rexistro!