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AAV9-Stathmin1 gene delivery improves disease phenotype in an intermediate mouse model of spinal muscular atrophy.
Villalón, E; Kline, R A; Smith, C E; Lorson, Z C; Osman, E Y; O'Day, S; Murray, L M; Lorson, C L.
Affiliation
  • Villalón E; Bond Life Sciences Center, University of Missouri, Columbia, MO 65211, USA.
  • Kline RA; Department of Veterinary Pathobiology, College of Veterinary Medicine, University of Missouri, Columbia, MO 65211, USA.
  • Smith CE; Bond Life Sciences Center, University of Missouri, Columbia, MO 65211, USA.
  • Lorson ZC; Department of Veterinary Pathobiology, College of Veterinary Medicine, University of Missouri, Columbia, MO 65211, USA.
  • Osman EY; Bond Life Sciences Center, University of Missouri, Columbia, MO 65211, USA.
  • O'Day S; Department of Veterinary Pathobiology, College of Veterinary Medicine, University of Missouri, Columbia, MO 65211, USA.
  • Murray LM; Bond Life Sciences Center, University of Missouri, Columbia, MO 65211, USA.
  • Lorson CL; Department of Veterinary Pathobiology, College of Veterinary Medicine, University of Missouri, Columbia, MO 65211, USA.
Hum Mol Genet ; 28(22): 3742-3754, 2019 11 15.
Article in En | MEDLINE | ID: mdl-31363739
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Muscular Atrophy, Spinal / Stathmin / Survival of Motor Neuron 1 Protein Limits: Animals Language: En Journal: Hum Mol Genet Year: 2019 Document type: Article
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Muscular Atrophy, Spinal / Stathmin / Survival of Motor Neuron 1 Protein Limits: Animals Language: En Journal: Hum Mol Genet Year: 2019 Document type: Article