Genes and mutations in human idiopathic epilepsy
Author:
Publisher
Elsevier BV
Subject
Clinical Neurology,Developmental Neuroscience,General Medicine,Pediatrics, Perinatology, and Child Health
Reference58 articles.
1. Autosomal dominant nocturnal frontal lobe epilepsy: a distinctive clinical disorder;Scheffer;Brain,1995
2. Autosomal dominant nocturnal frontal lobe epilepsy: electroclinical picture;Oldani;Epilepsia,1996
3. Autosomal dominant nocturnal frontal lobe epilepsy: demonstration of focal frontal onset and intrafamilial variation;Hayman;Neurology,1997
4. A missense mutation in the neuronal nicotinic acetylcholine receptor α4 subunit is associated with autosomal dominant nocturnal frontal lobe epilepsy;Steinlein;Nat Genet,1995
5. Independent occurrence of the CHRNA4 Ser248Phe mutation in a Norwegian family with nocturnal frontal lobe epilepsy;Steinlein;Epilepsia,2000
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