Molecular basis of the long-QT syndrome associated with deafness

N Engl J Med. 1997 May 29;336(22):1562-7. doi: 10.1056/NEJM199705293362204.
No abstract available

Publication types

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

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Aged, 80 and over
  • Child
  • Child, Preschool
  • Chromosomes, Human, Pair 11
  • DNA Mutational Analysis
  • Deafness / congenital
  • Deafness / genetics*
  • Female
  • Genetic Linkage
  • Homozygote
  • Humans
  • Infant
  • KCNQ Potassium Channels
  • KCNQ1 Potassium Channel
  • Long QT Syndrome / congenital
  • Long QT Syndrome / genetics*
  • Male
  • Middle Aged
  • Mutation
  • Pedigree
  • Potassium Channels / genetics*
  • Potassium Channels, Voltage-Gated*

Substances

  • KCNQ Potassium Channels
  • KCNQ1 Potassium Channel
  • KCNQ1 protein, human
  • Potassium Channels
  • Potassium Channels, Voltage-Gated

Associated data

  • GENBANK/U89364