SPG3A is the most frequent cause of hereditary spa... [Neurology. 2006] - PubMed

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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. [Hum Mutat. 2004]
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.
Atlastin1 mutations are frequent in young-onset autosomal dominant spastic paraplegia. [Arch Neurol. 2004]
Atlastin1 mutations are frequent in young-onset autosomal dominant spastic paraplegia.
Dürr A, Camuzat A, Colin E, Tallaksen C, Hannequin D, Coutinho P, Fontaine B, Rossi A, Gil R, Rousselle C, et al. Arch Neurol. 2004 Dec; 61(12):1867-72.
Clinical and genetic findings in a series of Italian children with pure hereditary spastic paraplegia. [Eur J Neurol. 2011]
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.
Review Hereditary spastic paraplegia: advances in genetic research. Hereditary Spastic Paraplegia Working group. [Neurology. 1996]
Review Hereditary spastic paraplegia: advances in genetic research. Hereditary Spastic Paraplegia Working group.
Fink JK, Heiman-Patterson T, Bird T, Cambi F, Dubé MP, Figlewicz DA, Fink JK, Haines JL, Heiman-Patterson T, Hentati A, et al. Neurology. 1996 Jun; 46(6):1507-14.
Review Hereditary spastic paraplegias: an update. [Curr Opin Neurol. 2007]
Review Hereditary spastic paraplegias: an update.
Depienne C, Stevanin G, Brice A, Durr A. Curr Opin Neurol. 2007 Dec; 20(6):674-80.

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Cited by 7 PubMed Central articles

Membrane fusion by the GTPase atlastin requires a conserved C-terminal cytoplasmic tail and dimerization through the middle domain. [Proc Natl Acad Sci U S A. 2011]
Membrane fusion by the GTPase atlastin requires a conserved C-terminal cytoplasmic tail and dimerization through the middle domain.
Moss TJ, Andreazza C, Verma A, Daga A, McNew JA. Proc Natl Acad Sci U S A. 2011 Jul 5; 108(27):11133-8. Epub 2011 Jun 20.
Review Fusing a lasting relationship between ER tubules. [Trends Cell Biol. 2011]
Review Fusing a lasting relationship between ER tubules.
Moss TJ, Daga A, McNew JA. Trends Cell Biol. 2011 Jul; 21(7):416-23. Epub 2011 May 6.
Mutational spectrum of the SPG4 (SPAST) and SPG3A (ATL1) genes in Spanish patients with hereditary spastic paraplegia. [BMC Neurol. 2010]
Mutational spectrum of the SPG4 (SPAST) and SPG3A (ATL1) genes in Spanish patients with hereditary spastic paraplegia.
Alvarez V, Sánchez-Ferrero E, Beetz C, Díaz M, Alonso B, Corao AI, Gámez J, Esteban J, Gonzalo JF, Pascual-Pascual SI, et al. BMC Neurol. 2010 Oct 8; 10:89. Epub 2010 Oct 8.

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SPG3A is the most frequent cause of hereditary spastic paraplegia with onset bef...
SPG3A is the most frequent cause of hereditary spastic paraplegia with onset before age 10 years.
Neurology. 2006 Jan 10 ;66(1):112-4.

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