Non-uniform dystrophin re-expression after CRISPR-mediated exon excision in the dystrophin/utrophin double-knockout mouse model of DMD

<div>Duchenne muscular dystrophy (DMD) is the most prevalent inherited myopathy affecting children, caused by genetic loss of the gene encoding the dystrophin protein. Here we have investigated the use of the&nbsp;<em>Staphylococcus aureus</em>&nbsp;CRISPR-Cas9 system and a...

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Bibliografische gegevens
Hoofdauteurs: Hanson, B, Stenler, S, Ahlskog, N, Chwalenia, K, Svrzikapa, N, Coenen-Stass, AML, Weinberg, MS, Wood, MJA, Roberts, TC
Formaat: Journal article
Taal:English
Gepubliceerd in: Cell Press 2022

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