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Read-through approach for stop mutations in Duchenne muscular dystrophy. An update
Dystrophinopathies are allelic conditions caused by deletions, duplications and point-mutations in the DMD gene, located on the X chromosome (Xp21.2). Mutations that prematurely interrupt the dystrophin protein synthesis lead to the most severe clinical form, Duchenne muscular Dystrophy, characteriz...
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Pacini Editore Srl
2021
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8033424/ https://www.ncbi.nlm.nih.gov/pubmed/33870095 http://dx.doi.org/10.36185/2532-1900-041 |