Multiple exon skipping and RNA circularisation contribute to the severe phenotypic expression of exon 5 dystrophin deletion

J Med Genet. 2003 Aug;40(8):e100. doi: 10.1136/jmg.40.8.e100.
No abstract available

Publication types

  • Multicenter Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alternative Splicing / genetics
  • Animals
  • Base Sequence
  • Dystrophin / genetics*
  • Exons / genetics*
  • Gene Deletion*
  • Gene Expression Regulation
  • Humans
  • Mice
  • Molecular Sequence Data
  • Muscular Dystrophy, Duchenne / genetics
  • Nucleic Acid Conformation
  • Phenotype
  • RNA / chemistry*
  • RNA / genetics*
  • RNA, Circular
  • Reading Frames / genetics

Substances

  • Dystrophin
  • RNA, Circular
  • RNA