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8. Mutation analysis of SPG4 and SPG3A genes and its implication in molecular diagnosis of Korean patients with hereditary spastic paraplegia. Park SY; Ki CS; Kim HJ; Kim JW; Sung DH; Kim BJ; Lee WY Arch Neurol; 2005 Jul; 62(7):1118-21. PubMed ID: 16009769 [TBL] [Abstract][Full Text] [Related]
9. Novel mutations in the Atlastin gene (SPG3A) in families with autosomal dominant hereditary spastic paraplegia and evidence for late onset forms of HSP linked to the SPG3A locus. Sauter SM; Engel W; Neumann LM; Kunze J; Neesen J Hum Mutat; 2004 Jan; 23(1):98. PubMed ID: 14695538 [TBL] [Abstract][Full Text] [Related]
10. Clinical and genetic findings in a series of Italian children with pure hereditary spastic paraplegia. Battini R; Fogli A; Borghetti D; Michelucci A; Perazza S; Baldinotti F; Conidi ME; Ferreri MI; Simi P; Cioni G Eur J Neurol; 2011 Jan; 18(1):150-7. PubMed ID: 20550563 [TBL] [Abstract][Full Text] [Related]
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