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Deletion of exon 26 of the dystrophin gene is associated with a mild Becker muscular dystrophy phenotype
With the possible introduction of exon skipping therapy in Duchenne muscular dystrophy, it has become increasingly important to know the role of each exon of the dystrophin gene to protein expression, and thus the phenotype. In this report, we present two related men with an unusually mild BMD assoc...
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| Main Authors: | , , |
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| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
Pacini Editore SpA
2011
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| Teme: | |
| Online dostop: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3298095/ https://ncbi.nlm.nih.gov/pubmed/22616200 |
| Oznake: |
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