Loading...
Corticostriatal dysfunction and glutamate transporter 1 (GLT1) in Huntington’s disease: interactions between neurons and astrocytes
Huntington’s Disease (HD) is a fatally inherited neurodegenerative disorder caused by an expanded glutamine repeat in the N-terminal region of the huntingtin (HTT) protein. The result is a progressively worsening triad of cognitive, emotional, and motor alterations that typically begin in adulthood...
Na minha lista:
| Main Authors: | , |
|---|---|
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
2012
|
| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3418680/ https://ncbi.nlm.nih.gov/pubmed/22905336 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.baga.2012.04.029 |
| Tags: |
Tilføj Tag
Ingen Tags, Vær først til at tagge denne postø!
|