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Functional conservation of human Spastin in a Drosophila model of autosomal dominant-hereditary spastic paraplegia
Mutations in spastin are the most frequent cause of the neurodegenerative disease autosomal dominant-hereditary spastic paraplegia (AD-HSP). Drosophila melanogaster lacking spastin exhibit striking behavioral similarities to human patients suffering from AD-HSP, suggesting conservation of Spastin fu...
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| Hauptverfasser: | , , , , |
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| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
Oxford University Press
2010
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2860889/ https://ncbi.nlm.nih.gov/pubmed/20154342 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddq064 |
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