[Contiguous gene deletion syndrome in Xp21]

Rev Neurol. 2010 Feb;50(3):192.
[Article in Spanish]
No abstract available

Publication types

  • Comment
  • Letter

MeSH terms

  • Adrenal Insufficiency / genetics
  • Adrenal Insufficiency / physiopathology
  • Chromosomes, Human, X / genetics*
  • Creatine Kinase / blood
  • Electromyography
  • Gene Deletion*
  • Genetic Diseases, X-Linked / genetics*
  • Genetic Diseases, X-Linked / physiopathology
  • Glycerol Kinase / genetics
  • Glycerol Kinase / metabolism
  • Humans
  • Infant
  • Muscular Dystrophy, Duchenne / genetics
  • Muscular Dystrophy, Duchenne / physiopathology
  • Syndrome

Substances

  • Glycerol Kinase
  • Creatine Kinase