Milder course in Duchenne patients with nonsense mutations and no muscle dystrophin
Neuromuscular Disorders2014Vol. 24(11), pp. 986–989
Citations Over TimeTop 10% of 2014 papers
Mayana Zatz, R.C.M. Pavanello, Monize Lazar, Guilherme Lopes Yamamoto, Naila Cristina Vilaça Lourenço, A. H. Cerqueira, Luciana Nogueira, Mariz Vainzof
Related Papers
- → Gentamicin treatment of Duchenne and Becker muscular dystrophy due to nonsense mutations(2001)259 cited
- → Jagged 1 Rescues the Duchenne Muscular Dystrophy Phenotype(2015)158 cited
- → What has the mdx mouse model of duchenne muscular dystrophy contributed to our understanding of this disease?(2015)75 cited
- → Somatic reversion/suppression of the mouse mdx phenotype in vivo(1990)273 cited
- Exon skipping prevents the onset of dystrophic pathology in the MDX mouse(2007)