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De novo <i>KCNQ2</i> mutations in patients with benign neonatal seizures
60
Citations
10
References
2004
Year
NeurophysiologyGenetic DisorderGeneticsPediatricsMolecular BiologyIon ChannelsFamily HistoryBenign Neonatal SeizuresNeonatal SeizuresNeuroscienceSpontaneous RemissionMedicinePotassium HomeostasisSocial SciencesNeurogenetics
Benign familial neonatal convulsions (BFNC) are characterized by unprovoked seizures during the first weeks of life with spontaneous remission after a few months. Mutations have been identified in the voltage-gated potassium ion channels KCNQ2 and KCNQ3. The authors performed a mutation analysis of KCNQ2 and KCNQ3 in six patients of whom four had no family history of neonatal seizures. The authors identified three KCNQ2 mutations in four patients that all arose de novo.
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