Idiopathic Epilepsies with a Monogenic Mode of Inheritance
Author:
Publisher
Wiley
Subject
Neurology (clinical),Neurology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1528-1157.1999.tb00892.x/fullpdf
Reference19 articles.
1. Proposal for Revised Classification of Epilepsies and Epileptic Syndromes.
2. A missense mutation in the neuronal nicotinic acetylcholine receptor α4 subunit is associated with autosomal dominant nocturnal frontal lobe epilepsy
3. A Potassium Channel Mutation in Neonatal Human Epilepsy
4. A novel potassium channel gene, KCNQ2, is mutated in an inherited epilepsy of newborns
5. A pore mutation in a novel KQT-like potassium channel gene in an idiopathic epilepsy family
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