Science · 1991 · 185 citations · 19 references
Life SciencesGeneticsMolecular GeneticsCytogeneticsEpilepsyNeurogeneticsEpilepsy GeneticsEtiology Of EpilepsyGene MappingGenetic EpilepsiesMolecular CytogeneticsMolecular NeurogeneticsGenetic Causes Of EpilepsyHereditary EpilepsiesInheritance Patterns In EpilepsyModifier Genes In EpilepsyProviral IntegrationSeizures
The neurological mutant mouse strain E1 is a model for complex partial seizures in humans. The inheritance of epileptic seizures with seven conventional chromosomal markers and over 60 endogenous proviral markers was studied by means of back-crosses of E1 with two seizure-resistant strains, DBA/2J and ABP/LeJ. The major gene responsible for this epileptic phenotype (El-1) was localized to a region distal with respect to the centromere on chromosome 9. At least one other gene, El-2, linked to proviral markers on chromosome 2, also influences the seizure phenotype. In addition, a potential modifier of seizures was detected in the DBA/2J background. The location of El-1 on distal chromosome 9 may allow identification of an epilepsy candidate gene in humans on the basis of conserved synteny with human chromosome 3.
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Mapping mendelian factors underlying quantitative traits using RFLP linkage maps.
Eric S. Lander, David Botstein · Genetics · 1989 · 5.3K citations · Full text
Life Sciences, Biology, Genetics +17
Linkage of Mls genes to endogenous mammary tumour viruses of inbred mice
Wayne N. Frankel, Christine K. Rudy, John M. Coffin et al. · Nature · 1991 · 306 citations