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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Autori principali: Rajendra, T.K., Gonsalvez, Graydon B., Walker, Michael P., Shpargel, Karl B., Salz, Helen K., Matera, A. Gregory
Natura: Artigo
Lingua:Inglês
Pubblicazione: The Rockefeller University Press 2007
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Research Articles
Accesso online: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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