Carregant...
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...
Guardat en:
| Publicat a: | Ann Neurol |
|---|---|
| Autors principals: | , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
2015
|
| Matèries: | |
| Accés en línia: | 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 |
| Etiquetes: |
Afegir etiqueta
Sense etiquetes, Sigues el primer a etiquetar aquest registre!
|