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Antisense oligonucleotides for the treatment of cardiomyopathy in Duchenne muscular dystrophy
Duchenne muscular dystrophy (DMD) is an X-linked recessive fatal neuromuscular disorder characterized by progressive muscle degeneration which affects one in 3500-5000 males born worldwide. DMD is caused by loss-of-function mutations in the dystrophin (DMD) gene encoding for dystrophin, a cytoskelet...
Uloženo v:
| Vydáno v: | Am J Transl Res |
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| Hlavní autoři: | , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
e-Century Publishing Corporation
2019
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6456507/ https://ncbi.nlm.nih.gov/pubmed/30972156 |
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