A novel mutation of KCNQ3 (c.925T→C) in a Japanese family with benign familial neonatal convulsions

Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

1. 1A novel mutation ofKCNQ3 (c.925T?C) in a Japanese family with benign familial neonatal convulsions2000 · 85 citations
2. 2Novel KCNQ3 Mutation in a Large Family with Benign Familial Neonatal Epilepsy: A Rare Cause of Neonatal Seizures2016 · 21 citations
3. 3A reduced K+ current due to a novel mutation in KCNQ2 causes neonatal convulsions1999 · 137 citations
4. 4A novel mutation in KCNQ2 associated with BFNC, drug resistant epilepsy, and mental retardation2004 · 156 citations
5. 5Two Novel KCNQ2 Mutations in 2 Families With Benign Familial Neonatal Convulsions2017 · 11 citations