Reply to "a novel mutation in the transmembrane 6 domain of GABBR2 leads to a rett-like phenotype"

Ann Neurol. 2018 Feb;83(2):439. doi: 10.1002/ana.25154.
No abstract available

Publication types

  • Letter
  • Comment

MeSH terms

  • Humans
  • Mutation
  • Phenotype*
  • Receptors, GABA-B / genetics
  • Rett Syndrome*

Substances

  • GABBR2 protein, human
  • Receptors, GABA-B