The 5' end of the KCNQ1OT1 gene is hypomethylated in the Beckwith-Wiedemann syndrome

Hum Genet. 2002 Jul;111(1):105-7. doi: 10.1007/s00439-002-0751-1. Epub 2002 Jun 14.
No abstract available

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 5' Untranslated Regions / genetics*
  • Beckwith-Wiedemann Syndrome / genetics*
  • CpG Islands
  • DNA Methylation
  • DNA Primers
  • Female
  • Genetic Predisposition to Disease
  • Genomic Imprinting
  • Humans
  • KCNQ Potassium Channels
  • KCNQ1 Potassium Channel
  • Long QT Syndrome / genetics
  • Male
  • Membrane Proteins*
  • Polymerase Chain Reaction
  • Potassium Channels / genetics*
  • Potassium Channels, Voltage-Gated*
  • Restriction Mapping

Substances

  • 5' Untranslated Regions
  • DNA Primers
  • KCNQ Potassium Channels
  • KCNQ1 Potassium Channel
  • KCNQ1 protein, human
  • KCNQ1OT1 long non-coding RNA, human
  • Membrane Proteins
  • Potassium Channels
  • Potassium Channels, Voltage-Gated