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Role of Astrocytes in the Pathophysiology of Lafora Disease and Other Glycogen Storage Disorders
Lafora disease is a rare disorder caused by loss of function mutations in either the EPM2A or NHLRC1 gene. The initial symptoms of this condition are most commonly epileptic seizures, but the disease progresses rapidly with dementia, neuropsychiatric symptoms, and cognitive deterioration and has a f...
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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MDPI
2023
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10000527/ https://www.ncbi.nlm.nih.gov/pubmed/36899857 http://dx.doi.org/10.3390/cells12050722 |