Hippocampal sclerosis worsens autosomal dominant nocturnal frontal lobe epilepsy ( ADNFLE ) phenotype related to CHRNB2 mutation
Author:
Affiliation:
1. Institute of Neurology University Magna Græcia Catanzaro Italy
2. Neuroimaging Research Unit National Research Council Catanzaro Italy
3. Institute of Neurological Sciences National Research Council, Mangone (CS) Italy
Publisher
Wiley
Subject
Neurology (clinical),Neurology
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1111/j.1468-1331.2012.03839.x
Reference13 articles.
1. The nicotinic receptor β2 subunit is mutant in nocturnal frontal lobe epilepsy
2. A new locus for autosomal dominant nocturnal frontal lobe epilepsy maps to chromosome 1
3. Further evidence of genetic heterogeneity in families with autosomal dominant nocturnal frontal lobe epilepsy
4. Dominant partial epilepsies: A clinical, electrophysiological and genetic study of 19 European families
5. Causes of epilepsies: Insights from discordant monozygous twins
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2. Sex differences in the nicotinic excitation of principal neurons within the developing hippocampal formation;Developmental Neurobiology;2018-12-14
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4. Generalized epilepsy in a family with basal ganglia calcifications and mutations in SLC20A2 and CHRNB2;European Journal of Medical Genetics;2015-11
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