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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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Detalhes bibliográficos
Main Authors: Du, Fang, Ozdowski, Emily F., Kotowski, Ingrid K., Marchuk, Douglas A., Sherwood, Nina Tang
Formato: Artigo
Idioma:Inglês
Publicado em: Oxford University Press 2010
Assuntos:
Acesso em linha: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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