A novel variant in YWHAG further supports phenotype of developmental and epileptic encephalopathy

Am J Med Genet A. 2021 May;185(5):1363-1365. doi: 10.1002/ajmg.a.62116. Epub 2021 Feb 15.
No abstract available

Publication types

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

MeSH terms

  • 14-3-3 Proteins / genetics
  • Brain Diseases*
  • Genetic Association Studies
  • Heterozygote
  • Humans
  • Mutation, Missense*
  • Phenotype

Substances

  • 14-3-3 Proteins
  • YWHAG protein, human