1. Localization of a gene for partial epilepsy to chromosome 10q
- Author
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Ottman, Ruth, Risch, Neil, Hauser, W. Allen, Pedley, Timothy A., Lee, Joseph H., Barker-Cummings, Christie, Lustenberger, Anita, Nagle, Keith J., Lee, Kyusang S., Scheuer, Mark L., Neystat, Michael, Susser, Mervyn, and Wilhelmsen, Kirk C.
- Abstract
There is strong evidence for a genetic contribution to epilepsy, but it is commonly assumed that this genetic contribution is limited to ‘generalized’ epilepsies, and that most forms of ‘partial’ epilepsy are nongenetic. In a linkage analysis of a single family containing 11 affected individuals, we obtained strong evidence for localization of a gene for partial epilepsy. This susceptibility gene maps to chromosome 10q, with a maximum two–point lod score for D10S192 of 3.99 at θ=0.0. All affected individuals share a single haplotype for seven tightly linked contiguous markers; the maximum lod score for this haplotype is 4.83 at θ=0.0. Key recombinants place the susceptibility locus within a 10 centimorgan interval.
- Published
- 1995
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