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.

Samankaltaisia teoksia

• Exon skipping induced by nonsense/frameshift mutations in DMD gene results in Becker muscular dystrophy
  Tekijä: Okubo, Mariko, et al.
  Julkaistu: (2020)
• 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.
  Tekijä: Hagiwara, Y., et al.
  Julkaistu: (1994)
• Dual exon skipping in myostatin and dystrophin for Duchenne muscular dystrophy
  Tekijä: Kemaladewi, Dwi U, et al.
  Julkaistu: (2011)
• Exon skipping during splicing of dystrophin mRNA precursor due to an intraexon deletion in the dystrophin gene of Duchenne muscular dystrophy kobe.
  Tekijä: Matsuo, M, et al.
  Julkaistu: (1991)
• Causes of clinical variability in Duchenne and Becker muscular dystrophies and implications for exon skipping therapies
  Tekijä: Hoffman, Eric P.
  Julkaistu: (2020)