Dystonia as a prominent feature of TCF20-associated neurodevelopmental disorder: Expanding the phenotype

Parkinsonism Relat Disord. 2022 Sep:102:89-91. doi: 10.1016/j.parkreldis.2022.07.026. Epub 2022 Aug 6.
No abstract available

Publication types

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

MeSH terms

  • Dystonia* / etiology
  • Dystonic Disorders* / genetics
  • Humans
  • Neurodevelopmental Disorders* / genetics
  • Phenotype
  • Transcription Factors / genetics

Substances

  • TCF20 protein, human
  • Transcription Factors