This Is very good news for gene therapy. 

Although this is not about DMD specifically, it can solve many of the problems. Like putting the sequence where its needed and the size of the dystrophy gene and just relpacing the missing pieces.

 

http://www.sciencedaily.com/releases/2011/06/110626145318.htm

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Looks very promising although it would suffer the same problems in that it would be an individualised personal medicine and would have to go through the same ringmarole that exon skipping is going through.

 

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