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Repression-free utrophin-A 5’UTR variants
Mutation in the dystrophin gene results Duchenne Muscular Dystrophy (DMD), an X-linked fatal neuromuscular disorder. Dystrophin deficiency can be compensated by upregulation of utrophin, an autosomal homologue of dystrophin. But the expression of utrophin in adults is restricted to myotendinous and...
Tallennettuna:
| Julkaisussa: | Mol Biol Res Commun |
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| Päätekijät: | , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Shiraz University
2019
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6802688/ https://ncbi.nlm.nih.gov/pubmed/31998814 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.22099/mbrc.2019.34240.1421 |
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