Novel missense mutation (G601S) of HERG in a Japanese long QT syndrome family

Hum Mutat. 1998:Suppl 1:S184-6. doi: 10.1002/humu.1380110159.
No abstract available

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Substitution
  • Cation Transport Proteins*
  • Codon / genetics
  • DNA / chemistry
  • DNA / genetics
  • DNA Mutational Analysis
  • DNA, Complementary / chemistry
  • DNA, Complementary / genetics
  • DNA-Binding Proteins*
  • ERG1 Potassium Channel
  • Ether-A-Go-Go Potassium Channels
  • Family Health
  • Glycine
  • Humans
  • Japan
  • Long QT Syndrome / genetics*
  • Long QT Syndrome / pathology
  • Mutation, Missense
  • Point Mutation
  • Polymorphism, Single-Stranded Conformational
  • Potassium Channels / genetics*
  • Potassium Channels, Voltage-Gated*
  • Serine
  • Trans-Activators*
  • Transcriptional Regulator ERG

Substances

  • Cation Transport Proteins
  • Codon
  • DNA, Complementary
  • DNA-Binding Proteins
  • ERG protein, human
  • ERG1 Potassium Channel
  • Ether-A-Go-Go Potassium Channels
  • KCNH2 protein, human
  • KCNH6 protein, human
  • Potassium Channels
  • Potassium Channels, Voltage-Gated
  • Trans-Activators
  • Transcriptional Regulator ERG
  • Serine
  • DNA
  • Glycine