Mutations in Kir2.1 Cause the Developmental and Episodic Electrical Phenotypes of Andersen's Syndrome

This publication has 43 references indexed in Scilit:

• Mapping of the Physical Interaction between the Intracellular Domains of an Inwardly Rectifying Potassium Channel, Kir6.2
  Published by Elsevier ,1999
• Mutations in the hminK gene cause long QT syndrome and suppress lKs function
  Nature Genetics, 1997
• Ontogeny of Gene Expression of Kir Channel Subunits in the Rat
  Molecular and Cellular Neuroscience, 1997
• Mutations in the ROMK Gene in Antenatal Bartter Syndrome Are Associated with Impaired K+Channel Function
  Biochemical and Biophysical Research Communications, 1997
• A potassium channel mutation in weaver mice implicates membrane excitability in granule cell differentiation
  Nature Genetics, 1995
• Calculation of QTc duration and variability in the presence of sinus arrhythmia
  The American Journal of Cardiology, 1995
• Molecular cloning and expression of a human heart inward rectifier potassium channel
  NeuroReport, 1994
• Molecular cloning and functional expression of a novel brain‐specific inward rectifier potassium channel
  FEBS Letters, 1994
• Circadian variation in the incidence of sudden cardiac death in the framingham heart study population
  The American Journal of Cardiology, 1987
• Sudden death risk in overt coronary heart disease: The Framingham Study
  American Heart Journal, 1987