BRD2 (RING3) Is a Probable Major Susceptibility Gene for Common Juvenile Myoclonic Epilepsy
- 1 August 2003
- journal article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 73 (2) , 261-270
- https://doi.org/10.1086/377006
Abstract
No abstract availableKeywords
This publication has 40 references indexed in Scilit:
- Channelopathies as a genetic cause of epilepsyCurrent Opinion in Neurology, 2003
- Truncation of the GABAA-Receptor γ2 Subunit in a Family with Generalized Epilepsy with Febrile Seizures PlusAmerican Journal of Human Genetics, 2002
- First genetic evidence of GABAA receptor dysfunction in epilepsy: a mutation in the γ2-subunit geneNature Genetics, 2001
- Genome scan of idiopathic generalized epilepsy: Evidence for major susceptibility gene and modifying genes influencing the seizure typeAnnals of Neurology, 2001
- Reproducibility and Complications in Gene Searches: Linkage on Chromosome 6, Heterogeneity, Association, and Maternal Inheritance in Juvenile Myoclonic EpilepsyAmerican Journal of Human Genetics, 2000
- Confirmation of linkage between juvenile myoclonic epilepsy locus and the HLA region of chromosome 6American Journal of Medical Genetics, 1991
- Juvenile myoclonic epilepsy (JME) may be linked to the BF and HLA loci on human chromosome 6American Journal of Medical Genetics, 1988
- Haplotype relative risks: an easy reliable way to construct a proper control sample for risk calculationsAnnals of Human Genetics, 1987
- Neuropathological Findings in Primary Generalized Epilepsy: A Study of Eight CasesEpilepsia, 1984
- Proposal for Revised Clinical and Electroencephalographic Classification of Epileptic SeizuresEpilepsia, 1981