Llwytho...
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...
Wedi'i Gadw mewn:
| Cyhoeddwyd yn: | Hum Mol Genet |
|---|---|
| Prif Awduron: | , , , , , , |
| Fformat: | Artigo |
| Iaith: | Inglês |
| Cyhoeddwyd: |
Oxford University Press
2018
|
| Pynciau: | |
| Mynediad Ar-lein: | 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 |
| Tagiau: |
Ychwanegu Tag
Dim Tagiau, Byddwch y cyntaf i dagio'r cofnod hwn!
|