Calmodulin mutations can underlie the phenotype of long QT syndrome variant 1

J Physiol. 2023 Sep;601(17):3695-3696. doi: 10.1113/JP285220. Epub 2023 Aug 9.
No abstract available

Keywords: CALM-2; IKS potassium channel; calmodulin; long QT syndrome.

Publication types

  • Comment

MeSH terms

  • Calmodulin* / genetics
  • Humans
  • KCNQ1 Potassium Channel / genetics
  • Long QT Syndrome* / genetics
  • Mutation
  • Phenotype

Substances

  • Calmodulin
  • KCNQ1 Potassium Channel