Marked hypotonia: An additional feature of ANO3-related movement disorder

Eur J Med Genet. 2022 Dec;65(12):104625. doi: 10.1016/j.ejmg.2022.104625. Epub 2022 Oct 10.
No abstract available

MeSH terms

  • Anoctamins / genetics
  • Dystonic Disorders*
  • Humans
  • Movement Disorders*
  • Muscle Hypotonia / genetics

Substances

  • Anoctamins
  • ANO3 protein, human