Translational readthrough by the aminoglycoside geneticin (G418) modulates SMN stability in vitro and improves motor function in SMA mice in vivo
Author:
Publisher
Oxford University Press (OUP)
Subject
Genetics(clinical),Genetics,Molecular Biology,General Medicine
Link
http://academic.oup.com/hmg/article-pdf/18/7/1310/17248628/ddp030.pdf
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4. An update of the mutation spectrum of the survival motor neuron gene (SMN1) in autosomal recessive spinal muscular atrophy (SMA);Wirth;Hum. Mutat.,2000
5. Determinants of exon 7 splicing in the spinal muscular atrophy genes, SMN1 and SMN2;Cartegni;Am. J. Hum. Genet.,2006
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