Mutation screen of the gene encoding GABRB3 in Chinese patients with childhood absence epilepsy

Am J Med Genet A. 2003 Dec 1;123A(2):197-200. doi: 10.1002/ajmg.a.20286.
No abstract available

Publication types

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

MeSH terms

  • Base Sequence
  • Child
  • China
  • DNA Mutational Analysis
  • Epilepsy, Absence / genetics*
  • Gene Frequency
  • Genetic Predisposition to Disease / genetics
  • Genotype
  • Humans
  • Molecular Sequence Data
  • Mutation / genetics*
  • Mutation, Missense / genetics
  • Polymorphism, Single Nucleotide / genetics
  • Receptors, GABA-A / genetics*
  • Sequence Analysis, DNA

Substances

  • Receptors, GABA-A