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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...
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| Publicado no: | Ann Neurol |
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| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2015
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| Assuntos: | |
| Acesso em linha: | 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 |
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