Loss-of-function mutations in the KCNJ8-Encoded Kir6.1 KATP channel and sudden infant death syndrome

Medicine & Life Sciences

• uK-ATP-1 potassium channel 100%
• KATP Channels 67%
• Sudden Infant Death 65%
• Loss of Function Mutation 59%
• Mutation 29%
• Pinacidil 15%
• Channelopathies 14%
• Premature Mortality 12%
• COS Cells 12%
• Sudden Death 10%
• Missense Mutation 10%
• DNA Sequence Analysis 10%
• Open Reading Frames 10%
• High Pressure Liquid Chromatography 8%
• Sepsis 8%
• Alleles 7%
• Polymerase Chain Reaction 6%
• Blood Vessels 6%
• DNA 5%
• Infections 5%
• Genes 4%