Advances on the Genetics of Mendelian Idiopathic Epilepsies
Author:
Publisher
Elsevier BV
Subject
Clinical Neurology
Reference109 articles.
1. A missense mutation in the neuronal nicotinic acetylcholine receptor alpha 4 subunit is associated with autosomal dominant nocturnal frontal lobe epilepsy;Steinlein;Nat Genet,1995
2. Mutations in LGI1 cause autosomal-dominant partial epilepsy with auditory features;Kalachikov;Nat Genet,2002
3. Mutations in the LGI1/Epitempin gene on 10q24 cause autosomal dominant lateral temporal epilepsy;Morante-Redolat;Hum Mol Genet,2002
4. Genetics of epilepsy syndromes starting in the first year of life;Deprez;Neurology,2009
5. A potassium channel mutation in neonatal human epilepsy;Biervert;Science,1998
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2. Are Changes in Synaptic Function That Underlie Hyperexcitability Responsible for Seizure Activity?;Issues in Clinical Epileptology: A View from the Bench;2014
3. Mutations inTNK2in severe autosomal recessive infantile onset epilepsy;Annals of Neurology;2013-09
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