[cite web | title = Entrez Gene: SPG3A spastic paraplegia 3A (autosomal dominant)| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=51062| accessdate = ] ] PBB_Summary
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References
Further reading
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*cite journal | author=Tessa A, Casali C, Damiano M, "et al." |title=SPG3A: An additional family carrying a new atlastin mutation. |journal=Neurology |volume=59 |issue= 12 |pages= 2002–5 |year= 2003 |pmid= 12499504 |doi=
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*cite journal | author=Zhu PP, Patterson A, Lavoie B, "et al." |title=Cellular localization, oligomerization, and membrane association of the hereditary spastic paraplegia 3A (SPG3A) protein atlastin. |journal=J. Biol. Chem. |volume=278 |issue= 49 |pages= 49063–71 |year= 2004 |pmid= 14506257 |doi= 10.1074/jbc.M306702200
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*cite journal | author=Sauter SM, Engel W, Neumann LM, "et al." |title=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. |journal=Hum. Mutat. |volume=23 |issue= 1 |pages= 98 |year= 2004 |pmid= 14695538 |doi= 10.1002/humu.9205
*cite journal | author=D'Amico A, Tessa A, Sabino A, "et al." |title=Incomplete penetrance in an SPG3A-linked family with a new mutation in the atlastin gene. |journal=Neurology |volume=62 |issue= 11 |pages= 2138–9 |year= 2004 |pmid= 15184642 |doi=
*cite journal | author=Hedera P, Fenichel GM, Blair M, Haines JL |title=Novel mutation in the SPG3A gene in an African American family with an early onset of hereditary spastic paraplegia. |journal=Arch. Neurol. |volume=61 |issue= 10 |pages= 1600–3 |year= 2004 |pmid= 15477516 |doi= 10.1001/archneur.61.10.1600
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*cite journal | author=Abel A, Fonknechten N, Hofer A, "et al." |title=Early onset autosomal dominant spastic paraplegia caused by novel mutations in SPG3A. |journal=Neurogenetics |volume=5 |issue= 4 |pages= 239–43 |year= 2005 |pmid= 15517445 |doi= 10.1007/s10048-004-0191-2
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