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- W2321000643 abstract "There has been much enthusiasm for the potential treatment of Duchenne muscular dystrophy over the past 15 years, ever since the discovery of the gene and the missing protein. This has expanded exponentially with successive experimental efforts at cell therapy, with myoblasts and multipotential stem cells, gene therapy, and now efforts at gene manipulation and gene repair. Animal models such as the dystrophin-deficient mdx mouse, have provided a useful experimental model in the laboratory but still left a considerable hiatus for clinical application." @default.
- W2321000643 created "2016-06-24" @default.
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- W2321000643 date "2006-01-01" @default.
- W2321000643 modified "2023-09-26" @default.
- W2321000643 title "THERAPEUTIC INNOVATIONS IN THE NEUROMUSCULAR DISORDERS" @default.
- W2321000643 doi "https://doi.org/10.1055/s-2006-945743" @default.
- W2321000643 hasPublicationYear "2006" @default.
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