Disruption of the splicing enhancer sequence within exon 27 of the dystrophin gene by a nonsense mutation induces partial skipping of the exon and is responsible for Becker muscular dystrophy.

Ítems similars

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• A novel point mutation (G-1 to T) in a 5' splice donor site of intron 13 of the dystrophin gene results in exon skipping and is responsible for Becker muscular dystrophy.
  per: Hagiwara, Y., et al.
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• Dual exon skipping in myostatin and dystrophin for Duchenne muscular dystrophy
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• Exon skipping during splicing of dystrophin mRNA precursor due to an intraexon deletion in the dystrophin gene of Duchenne muscular dystrophy kobe.
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• Causes of clinical variability in Duchenne and Becker muscular dystrophies and implications for exon skipping therapies
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