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Paraplegia, ISSN 0031-1758, 1963
Journal
2006, ISBN 0472115391, 246
Book
Journal Article
JOURNAL OF NEUROLOGY, ISSN 0340-5354, 01/2009, Volume 256, Issue 1, pp. 104 - 108
Autosomal recessive hereditary spastic paraplegia (AR HSP) with thin corpus callosum (TCC) is a rare neurodegenerative disorder often caused by mutations in... 
parkinsonism | MENTAL IMPAIRMENT | SPATACSIN | LOCUS | thin corpus callosum | PARAPARESIS | CLINICAL NEUROLOGY | spastic paraplegia | FAMILIES | GENETIC-HETEROGENEITY | MUTATIONS | SPG11 | THIN CORPUS-CALLOSUM | PROGRESSION
Journal Article
JAMA Neurology, ISSN 2168-6149, 07/2017, Volume 74, Issue 7, pp. 869 - 869
Journal Article
Brain, ISSN 0006-8950, 07/2016, Volume 139, Issue 7, pp. 1904 - 1918
Journal Article
Journal Article
PLoS ONE, ISSN 1932-6203, 08/2014, Volume 9, Issue 8, pp. e104790 - e104790
Journal Article
Cytoskeleton, ISSN 1949-3584, 04/2019, Volume 76, Issue 4, pp. 289 - 297
Mutations of the SPAST gene are the chief cause of hereditary spastic paraplegia. Controversy exists in the medical community as to whether the etiology of the... 
microtubule | gain‐of‐function | spastin | haploinsufficiency | HSP‐SPG4 | SPAST | hereditary spastic paraplegia | DEFECTS | MECHANISM | AXONAL-TRANSPORT | PHENOTYPES | MODEL | HSP-SPG4 | SPG4 | CELL BIOLOGY | RESCUE | gain-of-function | GENE DOSAGE | MUTATIONS | EXPRESSION | Hereditary spastic paraplegia | Proteins | Paraplegia | Animal models | Etiology | Paralysis | Pyramidal tracts | Mutation | Spastic paraplegia | Haploinsufficiency
Journal Article
Journal Article