Localization of a Gene for Benign Adult Familial Myoclonic Epilepsy to Chromosome 8q23.3-q24.1
- 1 September 1999
- journal article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 65 (3) , 745-751
- https://doi.org/10.1086/302535
Abstract
No abstract availableKeywords
Funding Information
- Ministry of Education, Culture, Sports, Science and Technology
- Japan Epilepsy Research Foundation
This publication has 34 references indexed in Scilit:
- Properties of neuronal nicotinic acetylcholine receptor mutants from humans suffering from autosomal dominant nocturnal frontal lobe epilepsyBritish Journal of Pharmacology, 1998
- Childhood Absence Epilepsy with Tonic-Clonic Seizures and Electroencephalogram 3–4-Hz Spike and Multispike–Slow Wave Complexes: Linkage to Chromosome 8q24American Journal of Human Genetics, 1998
- Familial cortical myoclonic tremor as a unique form of cortical reflex myoclonusMovement Disorders, 1997
- Suggestion of a major gene for familial febrile convulsions mapping to 8q13-21.Journal of Medical Genetics, 1996
- Localization of a Gene for a Glutamate Binding Subunit of a NMDA Receptor (GRINA) to 8q24Genomics, 1996
- Benign adult familial myoclonus epilepsy (BAFME): an autosomal dominant form not linked to the dentatorubral pallidoluysian atrophy (DRPLA) gene.Journal of Medical Genetics, 1996
- Localization of a gene for partial epilepsy to chromosome 10qNature Genetics, 1995
- Linkage Analysis between Familial Myoclonus Epilepsy and Short Arm of Chromosome 6 Using HLA Phenotype as Genetic MarkerPsychiatry and Clinical Neurosciences, 1993
- Incidence of Epilepsy and Unprovoked Seizures in Rochester, Minnesota: 1935–1984Epilepsia, 1993
- Cortical tremorNeurology, 1990