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PUBMED FOR HANDHELDS

Journal Abstract Search

141 related items for PubMed ID: 11704932

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  • 6. Hereditary spastic paraplegia: spastin phenotype and function.
    Fink JK, Rainier S.
    Arch Neurol; 2004 Jun; 61(6):830-3. PubMed ID: 15210518
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  • 11. Large deletion involving the 5'-UTR in the spastin gene caused mild phenotype of autosomal dominant hereditary spastic paraplegia.
    Iwanaga H, Tsujino A, Shirabe S, Eguchi H, Fukushima N, Niikawa N, Yoshiura K, Eguchi K.
    Am J Med Genet A; 2005 Feb 15; 133A(1):13-7. PubMed ID: 15637712
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  • 13. Intragenic modifiers of hereditary spastic paraplegia due to spastin gene mutations.
    Svenson IK, Kloos MT, Gaskell PC, Nance MA, Garbern JY, Hisanaga S, Pericak-Vance MA, Ashley-Koch AE, Marchuk DA.
    Neurogenetics; 2004 Sep 15; 5(3):157-64. PubMed ID: 15248095
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  • 14. Screening of patients with hereditary spastic paraplegia reveals seven novel mutations in the SPG4 (Spastin) gene.
    Proukakis C, Auer-Grumbach M, Wagner K, Wilkinson PA, Reid E, Patton MA, Warner TT, Crosby AH.
    Hum Mutat; 2003 Feb 15; 21(2):170. PubMed ID: 12552568
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  • 16. Hereditary spastic paraplegia caused by mutations in the SPG4 gene.
    Bürger J, Fonknechten N, Hoeltzenbein M, Neumann L, Bratanoff E, Hazan J, Reis A.
    Eur J Hum Genet; 2000 Oct 15; 8(10):771-6. PubMed ID: 11039577
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  • 20. A novel insertion mutation in spastin gene is the cause of spastic paraplegia in a Chinese family.
    Qin W, Zhang T, Han J, Tang L, Li X, Feng G, Liu W, He L.
    J Neurol Sci; 2003 Jun 15; 210(1-2):35-9. PubMed ID: 12736085
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