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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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| Publié dans: | Int J Mol Sci |
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| Auteurs principaux: | , , , , , , , |
| Format: | Artigo |
| Langue: | Inglês |
| Publié: |
MDPI
2020
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| Sujets: | |
| Accès en ligne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7589150/ https://ncbi.nlm.nih.gov/pubmed/33092303 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/ijms21207771 |
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