Xp21.2 contiguous gene syndrome due to deletion involving glycerol kinase and Duchenne muscular dystrophy loci

Neurol India. 2010 Jul-Aug;58(4):670-1. doi: 10.4103/0028-3886.68690.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Child, Preschool
  • Cognition Disorders / etiology
  • Glycerol Kinase / genetics*
  • Humans
  • Male
  • Muscular Dystrophy, Duchenne / complications
  • Muscular Dystrophy, Duchenne / genetics*
  • Sequence Deletion / genetics*

Substances

  • Glycerol Kinase