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Astrocytes: new players in progressive myoclonus epilepsy of Lafora type
Lafora disease (LD) is a fatal form of progressive myoclonus epilepsy characterized by the accumulation of insoluble poorly branched glycogen-like inclusions named Lafora bodies (LBs) in the brain and peripheral tissues. In the brain, since its first discovery in 1911, it was assumed that these glyc...
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| Publicat a: | Hum Mol Genet |
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| Autors principals: | , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Oxford University Press
2018
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6059194/ https://ncbi.nlm.nih.gov/pubmed/29408991 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddy044 |
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