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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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| 主要な著者: | , , , , , |
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| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
The Rockefeller University Press
2007
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| 主題: | |
| オンライン･アクセス: | 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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