In vitro evaluation of novel antisense oligonucleotides is predictive of in vivo exon skipping activity for Duchenne muscular dystrophy.

BACKGROUND: Targeted splice modulation of pre-mRNA transcripts by antisense oligonucleotides (AOs) can correct the function of aberrant disease-related genes. Duchenne muscular dystrophy (DMD) arises as a result of mutations that interrupt the open-reading frame in the DMD gene encoding dystrophin s...

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Détails bibliographiques
Auteurs principaux: Wang, Q, Yin, H, Camelliti, P, Betts, C, Moulton, H, Lee, H, Saleh, A, Gait, M, Wood, M
Format: Journal article
Langue:English
Publié: 2010