A pore mutation in a novel KQT-like potassium channel gene in an idiopathic epilepsy family

Biochemistry, Genetics and Molecular Biology

• Nested Gene 100%
• Chromosome 60%
• Mutation 40%
• Phenotype 20%
• Cloning 20%
• Potassium Channels 20%
• Inheritance 20%
• Autosomal Dominant Inheritance 20%
• Missense Mutation 20%
• Voltage-Gated Potassium Channel 20%
• Potassium Channel 20%
• Chromosome 8 20%
• Linkage Analysis 20%
• Genetic Heterogeneity 20%
• Hybrid 20%
• Radiation 20%
• Amino Acids 20%