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A Drosophila melanogaster model of spinal muscular atrophy reveals a function for SMN in striated muscle
Mutations in human survival motor neurons 1 (SMN1) cause spinal muscular atrophy (SMA) and are associated with defects in assembly of small nuclear ribonucleoproteins (snRNPs) in vitro. However, the etiological link between snRNPs and SMA is unclear. We have developed a Drosophila melanogaster syste...
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| Hlavní autoři: | , , , , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
The Rockefeller University Press
2007
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2064057/ https://ncbi.nlm.nih.gov/pubmed/17353360 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1083/jcb.200610053 |
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