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Causes of clinical variability in Duchenne and Becker muscular dystrophies and implications for exon skipping therapies
Becker muscular dystrophy is caused by mutations in the DMD gene that permit significant residual dystrophin protein expression in patient muscle. This is in contrast to DMD gene mutations in Duchenne muscular dystrophy where little or no dystrophin is produced (typically < 3% normal levels). Cli...
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Pacini Editore Srl
2020
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7783439/ https://www.ncbi.nlm.nih.gov/pubmed/33458572 http://dx.doi.org/10.36185/2532-1900-020 |