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Progress in Mapping Human Epilepsy Genes

1 Feb 1994

Abstract excerpt

The chromosomal loci for seven epilepsy genes have been identified in chromosomes 1q, 6p, 8q, 16p, 20q, 21q, and 22q. In 1987, the first epilepsy locus was mapped in a common benign idiopathic generalized epilepsy syndrome, juvenile myoclonic epilepsy (JME). Properdin factor or Bf, human leukocyte antigen (HLA), and DNA markers in the HLA-DQ region were genetically linked to JME and the locus, named EJM1, was...

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Identifiers

PMID: 8293722
DOI: 10.1111/j.1528-1157.1994.tb05926.x

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Related research

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Research trail→

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Progress in Mapping Human Epilepsy GenesPMID 8293722Read ↗

Refined mapping of the epilepsy susceptibility locus EJM1 on chromosome 6.Semantic proximity Read ↗

Mapping of genes predisposing to idiopathic generalized epilepsySemantic proximity Read ↗

Recent progress in the genetics of human epilepsies.Semantic proximity Read ↗

Gene mapping in the idiopathic generalized epilepsies: juvenile myoclonic epilepsy, childhood absence epilepsy, epilepsy with grand mal seizures, and early childhood myoclonic epilepsy.Semantic proximity Read ↗

Mutation analyses of genes on 6p12-p11 in patients with juvenile myoclonic epilepsy.Semantic proximity Read ↗

Advances in the genetics of progressive myoclonus epilepsy.Semantic proximity Read ↗

Advances in Genetics of Juvenile Myoclonic EpilepsiesSemantic proximity Read ↗

The phenotypic spectrum related to the human epilepsy susceptibility gene "EJM1".Semantic proximity Read ↗

Genetic mapping of a new Lafora progressive myoclonus epilepsy locus (<i>EPM2B</i>) on 6p22Semantic proximity Read ↗

Progress in the genetics of the partial epilepsies.Semantic proximity Read ↗

Remapping and mutation analysis of benign adult familial myoclonic epilepsy in a Japanese pedigree.Semantic proximity Read ↗

Exclusion of linkage of genetic focal sharp waves to the HLA region on chromosome 6p in families with benign partial epilepsy with centrotemporal sharp waves.Semantic proximity Read ↗

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