Rescue of severely affected dystrophin/utrophin-deficient mice through scAAV-U7snRNA-mediated exon skipping.

Duchenne muscular dystrophy (DMD) is a severe neuromuscular disorder caused by mutations in the dystrophin gene that result in the absence of functional protein. Antisense-mediated exon skipping is one of the most promising approaches for the treatment of DMD and recent clinical trials have demonstr...

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Detalhes bibliográficos
Principais autores: Goyenvalle, A, Babbs, A, Wright, J, Wilkins, V, Powell, D, Garcia, L, Davies, K
Formato: Conference item
Publicado em: 2012