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Therapeutic Strategies for Dystrophin Replacement in Duchenne Muscular Dystrophy
Duchenne muscular dystrophy (DMD) is an X-linked hereditary disease characterized by progressive muscle wasting due to modifications in the DMD gene (exon deletions, nonsense mutations, intra-exonic insertions or deletions, exon duplications, splice site defects, and deep intronic mutations) that re...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Frontiers Media S.A.
2022
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8995704/ https://www.ncbi.nlm.nih.gov/pubmed/35419381 http://dx.doi.org/10.3389/fmed.2022.859930 |