1. Genetic linkage analysis with dyslexia: evidence for linkage of spelling disability to chromosome 15.
- Author
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Nöthen MM, Schulte-Körne G, Grimm T, Cichon S, Vogt IR, Müller-Myhsok B, Propping P, and Remschmidt H
- Subjects
- Child, Chromosomes, Human, Pair 6, Dyslexia diagnosis, Genotype, Humans, Lod Score, Microsatellite Repeats genetics, Models, Genetic, Pedigree, Verbal Learning, Chromosome Mapping, Chromosomes, Human, Pair 15, Dyslexia genetics, Genetic Predisposition to Disease genetics
- Abstract
Dyslexia (reading and spelling disability) is one of the most frequently diagnosed disorders in childhood. Twin studies of dyslexia have indicated that deficits in spelling are substantially heritable and that the heritability of spelling deficits is higher than the heritability of reading deficits. We conducted a linkage study for spelling disability in seven multiplex families from Germany. Following previously reported linkage findings of components of dyslexia to chromosome 6p21-p22 and 15q21, we genotyped 26 microsatellite markers covering all of chromosome 6, and 13 microsatellite markers covering all of chromosome 15. While the chromosome 6 data were negative, results from chromosome 15 markers supported a locus on 15q21. The highest two-point LOD score was 1.26 with marker D15S143 at theta = 0. A multipoint LOD score of 1.78 (p = 0.0042) was achieved with a maximum at D15S132. Thus, our results provide independent support for a dyslexia gene on the long arm of chromosome 15.
- Published
- 1999
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