Nalaganje...
Hereditary Spastic Paraplegia-Linked REEP1 Modulates ER-Mitochondria Contacts
OBJECTIVE: Mutations in receptor expression enhancing protein 1 (REEP1) are associated with hereditary spastic paraplegias (HSPs). Although axonal degeneration is thought to be a predominant feature in HSP, the role of REEP1 mutations in degeneration is largely unknown. Previous studies have implica...
Shranjeno v:
| izdano v: | Ann Neurol |
|---|---|
| Main Authors: | , , , , |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
2015
|
| Teme: | |
| Online dostop: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4681538/ https://ncbi.nlm.nih.gov/pubmed/26201691 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ana.24488 |
| Oznake: |
Označite
Brez oznak, prvi označite!
|