Novel Mutation in KCNQ2 Causing Benign Familial Neonatal Seizures

Keyphrases

• Novel mutation 100%
• KCNQ2 100%
• Benign Familial Infantile Epilepsy 100%
• KCNQ3 40%
• M-current 40%
• KCNQ2 mutation 40%
• Seizure 20%
• Good Prognosis 20%
• Potassium Channel 20%
• Single-family 20%
• Neonatal Period 20%
• Complete Remission 20%
• Autosomal Dominant 20%
• DNA Testing 20%
• Mutation Type 20%
• Idiopathic Epilepsy 20%
• Channel Subunits 20%
• Neonatal Seizures 20%
• Benign Disease 20%
• Disease Prognosis 20%
• Chain Termination 20%
• KCNQ Genes 20%
• Single-strand Conformation Polymorphism 20%
• Polymorphism Analysis 20%
• Unaffected Family Members 20%

Medicine and Dentistry

• Benign Familial Neonatal Seizures 100%
• M Current 40%
• Epileptic Seizure 20%
• Newborn Period 20%
• Benign Tumor 20%
• Neonatal Infant 20%
• Physical Disease by Body Function 20%
• Generalised Epilepsy 20%
• Autosomal Dominant Inheritance 20%
• Sanger Sequencing 20%
• Infantile Spasm 20%
• Potassium Channel 20%
• Diseases 20%
• Neonatal Period 20%

Neuroscience

• Benign Familial Neonatal Seizures 100%
• M Current 40%
• Potassium Channel 20%
• Generalised Epilepsy 20%
• Dideoxynucleotide Sequencing 20%