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Strumpellin and Spartin, Hereditary Spastic Paraplegia Proteins, are Binding Partners
Hereditary spastic paraplegia (HSP) is one of the most heterogeneous neurodegenerative diseases with more than 50 identified genes causing a relatively stereotypical phenotypic presentation. Recent studies of HSP pathogenesis have suggested the existence of shared biochemical pathways that are cruci...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Libertas Academica
2015
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4426939/ https://www.ncbi.nlm.nih.gov/pubmed/25987849 http://dx.doi.org/10.4137/JEN.S22969 |