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18) Vazza G, Zortea M, Boaretto F, et al. A new locus for autosomal recessive spastic paraplegia associated with mental retardation and distal motor neuropathy, SPG14, maps to chromosome 3q27-q28. Am J Hum Genet. 2000; 67: 504-9
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19) Hughes CA, Byrne PC, Webb S, et al. SPG15, a new locus for autosomal recessive complicated HSP on chromosome 14q. Neurology 2001; 56: 1230-3
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33) Engert JC, Berube P, Mercier J, et al. ARSACS, a spastic ataxia common in northeastern Quebec, is caused by mutations in a new gene encoding an 11. 5-kb ORF. Nat Genet. 2000; 24: 120-5
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38) Durr A, Camuzat A, Colin E, et al. Atlastin 1 mutations are frequent in young-onset autosomal dominant spastic paraplegia. Arch Neurol. 2004; 61: 1867-72
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