Delineating a new critical region for juvenile myoclonic epilepsy at the 22q11.2 chromosome

Epilepsy Behav. 2013 Dec;29(3):587-8. doi: 10.1016/j.yebeh.2013.08.008. Epub 2013 Sep 5.
No abstract available

Publication types

  • Letter

MeSH terms

  • Chromosome Disorders / complications
  • Chromosome Disorders / genetics
  • Chromosomes, Human, Pair 21*
  • Humans
  • Mutation / genetics
  • Myoclonic Epilepsy, Juvenile / etiology
  • Myoclonic Epilepsy, Juvenile / genetics*
  • rab GTP-Binding Proteins / genetics

Substances

  • Rab36 protein, human
  • rab GTP-Binding Proteins