A novel mutation ofKCNQ3 (c.925T?C) in a Japanese family with benign familial neonatal convulsions

Also Consider

Synapse has enriched 3 closely related papers on similar clinical questions. Consider them for comparative context:

1. 1A Potassium Channel Mutation in Neonatal Human Epilepsy1998 · 1,089 citations
2. 2Functional Expression of Two KvLQT1-related Potassium Channels Responsible for an Inherited Idiopathic Epilepsy1998 · 200 citations
3. 3Analysis of any point mutation in DNA. The amplification refractory mutation system (ARMS)1989 · 2,517 citations