Autosomal Dominant Nocturnal Frontal-Lobe Epilepsy: Genetic Heterogeneity and Evidence for a Second Locus at 15q24
- 1 October 1998
- journal article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 63 (4) , 1108-1116
- https://doi.org/10.1086/302047
Abstract
No abstract availableKeywords
This publication has 40 references indexed in Scilit:
- SSCP variants within the α4 subunit of the neuronal nicotinic acetylcholine receptor geneClinical Genetics, 2008
- Short Report on DNA Marker at Candidate Locus: Dinucleotide polymorphism in the first intron of the human neuronal nicotinic acetylcholine receptor α4 subunit gene (CHRNA4)Clinical Genetics, 2008
- Familial Infantile Convulsions and Paroxysmal Choreoathetosis: A New Neurological Syndrome Linked to the Pericentromeric Region of Human Chromosome 16American Journal of Human Genetics, 1997
- Epilepsies with single gene inheritanceBrain & Development, 1997
- An amino acid exchange in the second transmembrane segment of a neuronal nicotinic receptor causes partial epilepsy by altering its desensitization kineticsFEBS Letters, 1996
- Suggestion of a major gene for familial febrile convulsions mapping to 8q13-21.Journal of Medical Genetics, 1996
- Exon–Intron Structure of the Human Neuronal Nicotinic Acetylcholine Receptor α4 Subunit (CHRNA4)Genomics, 1996
- Autosomal dominant frontal epilepsy misdiagnosed as sleep disorderThe Lancet, 1994
- Benign familial neonatal convulsions linked to genetic markers on chromosome 20Nature, 1989
- cDNA clones coding for the structural subunit of a chicken brain nicotinic acetylcholine receptorNeuron, 1988