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Brain, ISSN 0006-8950, 07/2016, Volume 139, Issue 7, pp. 1904 - 1918
Journal Article
Autophagy, ISSN 1554-8627, 01/2019, Volume 15, Issue 1, pp. 34 - 57
ZFYVE26/Spastizin and SPG11/Spatacsin encode 2 large proteins that are mutated in hereditary autosomal-recessive spastic paraplegia/paraparesis (HSP) type 15... 
RAB11 | AR-SPG11 | ZFYVE26 | autophagy | endocytosis | RAB5A | SPG11 | AR-SPG15 | autophagosome-endosome fusion | COMPLEX | RAB5 | SPATACSIN | MATURATION | CELL BIOLOGY | MULTIVESICULAR BODIES | EARLY ENDOSOMES | PROTEINS | THIN CORPUS-CALLOSUM | EGF RECEPTOR
Journal Article
Journal Article
Human mutation, ISSN 1059-7794, 2009, Volume 30, Issue 3, pp. E500 - E519
Journal Article
Annals of Neurology, ISSN 0364-5134, 05/2016, Volume 79, Issue 5, pp. 826 - 840
Objective: Mutations in the spastic paraplegia gene 11 (SPG11), encoding spatacsin, cause the most frequent form of autosomal-recessive complex hereditary... 
CYTOKINESIS | DEFECTS | GENE | HEREDITARY SPASTIC PARAPLEGIA | PROLIFERATION | SPATACSIN | MUTATIONS | THIN CORPUS-CALLOSUM | SPG11 | NEUROSCIENCES | PROGRESSION | CLINICAL NEUROLOGY
Journal Article
Journal of Clinical Neuroscience, ISSN 0967-5868, 09/2019, Volume 67, pp. 19 - 23
Hereditary Spastic paraplegias (HSPs) are heterogeneous group of degenerative disorders characterized by progressive weakness and spasticity of the lower... 
Ataxia | SPG56 | Spastic paraplegia | Peripheral neuropathy | SPG11 | Biotechnology | Anopheles | Molecular genetics | Paralysis, Spastic | Genes | Genetically modified organisms | Cytochrome P-450 | Genetic engineering | Nucleotide sequencing | DNA sequencing | Index Medicus
Journal Article
European journal of human genetics, ISSN 1018-4813, 2013, Volume 21, Issue 11, pp. 1312 - 1315
Journal Article