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- W215369708 abstract "The hereditary spastic paraplegias (HSPs) are among the most genetically diverse neurological disorders, with almost 60 distinct genetic loci already mapped and over 30 genes identified. Though a majority of HSP cases reflect autosomal dominant inheritance, a larger number of genes have been identified mediating various autosomal recessive forms. Importantly, a number of mouse models have been generated for these recessive forms to model loss-of-function mechanisms, using mainly homologous recombination-based, gene knockout approaches. These models are proving to be valuable tools for clarifying the pathophysiologic mechanisms underlying the HSPs and for evaluating new therapies." @default.
- W215369708 created "2016-06-24" @default.
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- W215369708 date "2015-01-01" @default.
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- W215369708 title "Murine Models of Autosomal Recessive Hereditary Spastic Paraplegia" @default.
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- W215369708 doi "https://doi.org/10.1016/b978-0-12-405195-9.00071-8" @default.
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