Á lódáil...
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...
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| Foilsithe in: | Mol Biol Res Commun |
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| Main Authors: | , |
| Formáid: | Artigo |
| Teanga: | Inglês |
| Foilsithe: |
Shiraz University
2019
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| Ábhair: | |
| Rochtain Ar Líne: | 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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