Nalaganje...
A role for cerebellum in the hereditary dystonia DYT1
DYT1 is a debilitating movement disorder caused by loss-of-function mutations in torsinA. How these mutations cause dystonia remains unknown. Mouse models which have embryonically targeted torsinA have failed to recapitulate the dystonia seen in patients, possibly due to differential developmental c...
Shranjeno v:
| izdano v: | eLife |
|---|---|
| Main Authors: | , , , |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
eLife Sciences Publications, Ltd
2017
|
| Teme: | |
| Online dostop: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5340526/ https://ncbi.nlm.nih.gov/pubmed/28198698 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.7554/eLife.22775 |
| Oznake: |
Označite
Brez oznak, prvi označite!
|