Gene symbol: KCNQ1

Hum Genet. 2007 Feb;120(6):912.
No abstract available

Publication types

  • Case Reports

MeSH terms

  • Amino Acid Substitution
  • Case-Control Studies
  • Child
  • Female
  • Humans
  • KCNQ1 Potassium Channel / genetics*
  • Long QT Syndrome / genetics*
  • Mutation, Missense

Substances

  • KCNQ1 Potassium Channel
  • KCNQ1 protein, human