Cellular distribution and subcellular localization of spatacsin and spastizin, two proteins involved in hereditary spastic paraplegia
- 30 June 2011
- journal article
- research article
- Published by Elsevier BV in Molecular and Cellular Neuroscience
- Vol. 47 (3), 191-202
- https://doi.org/10.1016/j.mcn.2011.04.004
Abstract
No abstract availableKeywords
This publication has 40 references indexed in Scilit:
- A Genome-Scale DNA Repair RNAi Screen Identifies SPG48 as a Novel Gene Associated with Hereditary Spastic ParaplegiaPLoS Biology, 2010
- SPG15 is the second most common cause of hereditary spastic paraplegia with thin corpus callosumNeurology, 2009
- Spastic paraplegia with thinning of the corpus callosum and white matter abnormalities: Further mutations and relative frequency in ZFYVE26/SPG15 in the Italian populationJournal of the Neurological Sciences, 2009
- Identification of a heterozygous genomic deletion in the spatacsin gene in SPG11 patients using high-resolution comparative genomic hybridizationneurogenetics, 2008
- SPG11 mutations are common in familial cases of complicated hereditary spastic paraplegiaNeurology, 2008
- Identification of the SPG15 Gene, Encoding Spastizin, as a Frequent Cause of Complicated Autosomal-Recessive Spastic Paraplegia, Including Kjellin SyndromeAmerican Journal of Human Genetics, 2008
- Traffic accidents: Molecular genetic insights into the pathogenesis of the hereditary spastic paraplegiasPharmacology & Therapeutics, 2006
- The extent of axonal loss in the long tracts in hereditary spastic paraplegiaNeuropathology and Applied Neurobiology, 2004
- Is the Transportation Highway the Right Road for Hereditary Spastic Paraplegia?American Journal of Human Genetics, 2002
- The neuropathology of hereditary spastic paraparesisClinical Neurology and Neurosurgery, 1992