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9. Novel mutations of the SPG11 gene in hereditary spastic paraplegia with thin corpus callosum. Liao SS; Shen L; Du J; Zhao GH; Wang XY; Yang Y; Xiao ZQ; Yuan Y; Jiang H; Li N; Sun HD; Wang JL; Wang CY; Zhou YF; Mo XY; Xia K; Tang BS J Neurol Sci; 2008 Dec; 275(1-2):92-9. PubMed ID: 18835492 [TBL] [Abstract][Full Text] [Related]
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13. SPG11 mutations cause Kjellin syndrome, a hereditary spastic paraplegia with thin corpus callosum and central retinal degeneration. Orlén H; Melberg A; Raininko R; Kumlien E; Entesarian M; Söderberg P; Påhlman M; Darin N; Kyllerman M; Holmberg E; Engler H; Eriksson U; Dahl N Am J Med Genet B Neuropsychiatr Genet; 2009 Oct; 150B(7):984-92. PubMed ID: 19194956 [TBL] [Abstract][Full Text] [Related]
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16. Chinese families with autosomal recessive hereditary spastic paraplegia caused by mutations in SPG11. Chen X; Liu J; Wei QQ; Ou RW; Cao B; Yuan X; Hou Y; Zhang L; Shang H BMC Neurol; 2020 Jan; 20(1):2. PubMed ID: 31900114 [TBL] [Abstract][Full Text] [Related]
17. Novel Compound Heterozygous Spatacsin Mutations in a Greek Kindred with Hereditary Spastic Paraplegia SPG11 and Dementia. Fraidakis MJ; Brunetti M; Blackstone C; Filippi M; Chiò A Neurodegener Dis; 2016; 16(5-6):373-81. PubMed ID: 27318863 [TBL] [Abstract][Full Text] [Related]
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