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256 related items for PubMed ID: 24824479

  • 1. Spastin mutation screening in Chinese patients with pure hereditary spastic paraplegia.
    Wei QQ, Chen Y, Zheng ZZ, Chen X, Huang R, Yang Y, Burgunder J, Shang HF.
    Parkinsonism Relat Disord; 2014 Aug; 20(8):845-9. PubMed ID: 24824479
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  • 2. Exon 8-17 deletions of SPAST in a Chinese family with hereditary spastic paraplegia: a case report and literature review.
    Wang K, Zhao G.
    J Neurol Sci; 2015 Oct 15; 357(1-2):282-4. PubMed ID: 26165777
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  • 3. Genetic analysis of SPG4 and SPG3A genes in a cohort of Chinese patients with hereditary spastic paraplegia.
    Lu X, Cen Z, Xie F, Ouyang Z, Zhang B, Zhao G, Luo W.
    J Neurol Sci; 2014 Dec 15; 347(1-2):368-71. PubMed ID: 25454648
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  • 7. Two novel mutations in the Spastin gene of Chinese patients with hereditary spastic paraplegia.
    Fei QZ, Tang WG, Rong TY, Tang HD, Liu JR, Guo ZL, Fu Y, Xiao Q, Wang XJ, He SB, Cao L, Chen SD.
    Eur J Neurol; 2011 Sep 15; 18(9):1194-6. PubMed ID: 21834905
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  • 9. A novel SPAST gene mutation identified in a Chinese family with hereditary spastic paraplegia.
    Yu W, Jin H, Deng J, Nan D, Huang Y.
    BMC Med Genet; 2020 Jun 03; 21(1):123. PubMed ID: 32493220
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  • 10. High frequency of partial SPAST deletions in autosomal dominant hereditary spastic paraplegia.
    Beetz C, Nygren AO, Schickel J, Auer-Grumbach M, Bürk K, Heide G, Kassubek J, Klimpe S, Klopstock T, Kreuz F, Otto S, Schüle R, Schöls L, Sperfeld AD, Witte OW, Deufel T.
    Neurology; 2006 Dec 12; 67(11):1926-30. PubMed ID: 17035675
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  • 11. 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, López de Munain A, Moris G, Ribacoba R, Márquez C, Rosell J, Marín R, García-Barcina MJ, Del Castillo E, Benito C, Coto E, Group for the Study of the Genetics of Spastic Paraplegia.
    BMC Neurol; 2010 Oct 08; 10():89. PubMed ID: 20932283
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  • 18. Hereditary spastic paraplegia due to SPAST mutations in 151 Dutch patients: new clinical aspects and 27 novel mutations.
    de Bot ST, van den Elzen RT, Mensenkamp AR, Schelhaas HJ, Willemsen MA, Knoers NV, Kremer HP, van de Warrenburg BP, Scheffer H.
    J Neurol Neurosurg Psychiatry; 2010 Oct 08; 81(10):1073-8. PubMed ID: 20562464
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  • 20. Expansion of mutation spectrum, determination of mutation cluster regions and predictive structural classification of SPAST mutations in hereditary spastic paraplegia.
    Shoukier M, Neesen J, Sauter SM, Argyriou L, Doerwald N, Pantakani DV, Mannan AU.
    Eur J Hum Genet; 2009 Feb 08; 17(2):187-94. PubMed ID: 18701882
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