Hypothesis: the existence of embryonic and adult isoforms of mRNA dystrophin provides an explanation for unusual clinical findings

Am J Med Genet. 1989 Mar;32(3):438-41. doi: 10.1002/ajmg.1320320336.
No abstract available

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Dystrophin
  • Gene Expression Regulation
  • Humans
  • Infant
  • Male
  • Muscle Proteins / genetics*
  • Muscular Dystrophies / embryology
  • Muscular Dystrophies / genetics*
  • Muscular Dystrophies / pathology
  • Phenotype
  • RNA, Messenger / biosynthesis
  • RNA, Messenger / genetics
  • Stereoisomerism

Substances

  • Dystrophin
  • Muscle Proteins
  • RNA, Messenger