Autosomal dominant nocturnal frontal lobe epilepsy

Epilepsia

Volumn 41, Issue 8, 2000, Pages 1059-1060

  Scheffer, I E ^a  

^a UNIVERSITY OF MELBOURNE   (Australia)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; AUTOSOMAL DOMINANT DISORDER; CLINICAL FEATURE; ELECTROENCEPHALOGRAPHY; FRONTAL LOBE EPILEPSY; GENETIC ANALYSIS; GENETIC LINKAGE; HUMAN; ONSET AGE; PRIORITY JOURNAL;

EID: 0033892736     PISSN: 00139580     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1528-1157.2000.tb00298.x     Document Type: Article

References (13)

1. Autosomal dominant frontal epilepsy misdiagnosed as sleep disorder
2. 4 subunit is associated with autosomal dominant nocturnal frontal lobe epilepsy
3. 1 subunit gene SCN1B
4. Autosomal dominant nocturnal frontal lobe epilepsy: A distinctive clinical disorder
5. Autosomal dominant nocturnal frontal lobe epilepsy: Electroclinical picture
6. Nocturnal frontal lobe epilepsy: A clinical and polygraphic overview of 100 consecutive cases
7. Autosomal dominant nocturnal frontal lobe epilepsy: Demonstration of focal frontal onset and intrafamilial variation
8. Localization of a gene for autosomal dominant nocturnal frontal lobe epilepsy to chromosome 20q13.2
9. Autosomal dominant nocturnal frontal lobe epilepsy: Genetic heterogeneity and a probable second locus at 15q24
10. An insertion mutation of the CHRNA4 gene in a family with autosomal dominant nocturnal frontal lobe epilepsy
11. An amino acid exchange in the second transmembrane segment of a neuronal nicotinic receptor causes partial epilepsy by altering its desensitization kinetics
12. Properties of neuronal nicotinic acetylcholine receptor mutants from humans suffering from autosomal dominant nocturnal frontal lobe epilepsy
13. Neuronal nicotinic acetylcholine receptor and epilepsy