Splicing analysis disclosed a determinant single nucleotide for exon skipping caused by a novel intraexonic four‐nucleotide deletion in the dystrophin gene

Lignende værker

• Chemical treatment enhances skipping of a mutated exon in the dystrophin gene
  af: Nishida, Atsushi, et al.
  Udgivet: (2011)
• Exon skipping during splicing of dystrophin mRNA precursor due to an intraexon deletion in the dystrophin gene of Duchenne muscular dystrophy kobe.
  af: Matsuo, M, et al.
  Udgivet: (1991)
• 2′-O-Methyl RNA/Ethylene-Bridged Nucleic Acid Chimera Antisense Oligonucleotides to Induce Dystrophin Exon 45 Skipping
  af: Lee, Tomoko, et al.
  Udgivet: (2017)
• Categorization of 77 dystrophin exons into 5 groups by a decision tree using indexes of splicing regulatory factors as decision markers
  af: Malueka, Rusdy Ghazali, et al.
  Udgivet: (2012)
• 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.
  af: Shiga, N, et al.
  Udgivet: (1997)