Channelopathies as a genetic cause of epilepsy
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Clinical Neurology,Neurology
Reference47 articles.
1. A missense mutation in the neuronal nicotinic acetylcholine receptor α4 subunit is associated with autosomal dominant nocturnal frontal lobe epilepsy
2. A Potassium Channel Mutation in Neonatal Human Epilepsy
3. A novel potassium channel gene, KCNQ2, is mutated in an inherited epilepsy of newborns
4. Myokymia and neonatal epilepsy caused by a mutation in the voltage sensor of the KCNQ2 K+ channel
5. A pore mutation in a novel KQT-like potassium channel gene in an idiopathic epilepsy family
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