Caricamento...
Molecular mechanisms underlying Spinocerebellar Ataxia 17 (SCA17) pathogenesis
Spinocerebellar ataxia 17 (SCA17) belongs to the family of 9 genetically inherited, late-onset neurodegenerative diseases, which are caused by polyglutamine (polyQ) expansion in different proteins. In SCA17, the polyQ expansion occurs in the TATA box binding protein (TBP), which functions as a gener...
Salvato in:
| Pubblicato in: | Rare Dis |
|---|---|
| Autori principali: | , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Taylor & Francis
2016
|
| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5154381/ https://ncbi.nlm.nih.gov/pubmed/28032013 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1080/21675511.2016.1223580 |
| Tags: |
Aggiungi Tag
Nessun Tag, puoi essere il primo ad aggiungerne! !
|