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Journal Abstract Search

973 related items for PubMed ID: 18178576

  • 21. Robust quantification of the SMN gene copy number by real-time TaqMan PCR.
    Gómez-Curet I, Robinson KG, Funanage VL, Crawford TO, Scavina M, Wang W.
    Neurogenetics; 2007 Nov; 8(4):271-8. PubMed ID: 17647030
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  • 30. Spinal muscular atrophy: from gene to therapy.
    Wirth B, Brichta L, Hahnen E.
    Semin Pediatr Neurol; 2006 Jun; 13(2):121-31. PubMed ID: 17027862
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  • 32. Investigation of the role of SMN1 and SMN2 haploinsufficiency as a risk factor for Hirayama's disease: clinical, neurophysiological and genetic characteristics in a Spanish series of 13 patients.
    Gamez J, Also E, Alias L, Corbera-Bellalta M, Barceló MJ, Centeno M, Raguer N, Gratacós M, Baiget M, Tizzano EF.
    Clin Neurol Neurosurg; 2007 Dec; 109(10):844-8. PubMed ID: 17850955
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  • 35. Implication of fetal SMN2 expression in type I SMA pathogenesis: protection or pathological gain of function?
    Soler-Botija C, Cuscó I, Caselles L, López E, Baiget M, Tizzano EF.
    J Neuropathol Exp Neurol; 2005 Mar; 64(3):215-23. PubMed ID: 15804053
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  • 38. Correction of SMN2 Pre-mRNA splicing by antisense U7 small nuclear RNAs.
    Madocsai C, Lim SR, Geib T, Lam BJ, Hertel KJ.
    Mol Ther; 2005 Dec; 12(6):1013-22. PubMed ID: 16226920
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  • 39. Refined characterization of the expression and stability of the SMN gene products.
    Vitte J, Fassier C, Tiziano FD, Dalard C, Soave S, Roblot N, Brahe C, Saugier-Veber P, Bonnefont JP, Melki J.
    Am J Pathol; 2007 Oct; 171(4):1269-80. PubMed ID: 17717146
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