Genetic mechanisms that underlie epilepsy
- 1 May 2004
- journal article
- review article
- Published by Springer Nature in Nature Reviews Neuroscience
- Vol. 5 (5) , 400-408
- https://doi.org/10.1038/nrn1388
Abstract
No abstract availableThis publication has 75 references indexed in Scilit:
- Sodium-channel defects in benign familial neonatal-infantile seizuresThe Lancet, 2002
- Mutations in LGI1 cause autosomal-dominant partial epilepsy with auditory featuresNature Genetics, 2002
- A missense mutation of the Na + channel α II subunit gene Na v 1.2 in a patient with febrile and afebrile seizures causes channel dysfunctionProceedings of the National Academy of Sciences, 2001
- The nicotinic receptor β2 subunit is mutant in nocturnal frontal lobe epilepsyNature Genetics, 2000
- Mutations of SCN1A, encoding a neuronal sodium channel, in two families with GEFS+2Nature Genetics, 2000
- Febrile seizures and generalized epilepsy associated with a mutation in the Na+-channel ß1 subunit gene SCN1BNature Genetics, 1998
- A Potassium Channel Mutation in Neonatal Human EpilepsyScience, 1998
- A pore mutation in a novel KQT-like potassium channel gene in an idiopathic epilepsy familyNature Genetics, 1998
- A novel potassium channel gene, KCNQ2, is mutated in an inherited epilepsy of newbornsNature Genetics, 1998
- A missense mutation in the neuronal nicotinic acetylcholine receptor α4 subunit is associated with autosomal dominant nocturnal frontal lobe epilepsyNature Genetics, 1995