Article
The Friedreich ataxia gene is assigned to chromosome 9q13-q21 by mapping of tightly linked markers and shows linkage disequilibrium with D9S15.
American journal of human genetics - 1 Jan 1990
Hanauer A, Chery M, Fujita R, Driesel A J, Gilgenkrantz S, Mandel J L
Abstract excerpt
Chamberlain et al. have assigned the gene for Friedreich ataxia (FA), a recessive neurodegenerative disorder, to chromosome 9, and have proposed a regional localization in the proximal short arm (9p22-cen), on the basis of linkage to D9S15 and to interferon-beta (IFNB), the latter being localized...
Topics
- Alleles
- Chromosome Banding
- Chromosome Mapping
- Chromosomes, Human, Pair 9
- DNA Probes
- Friedreich Ataxia
- Gene Frequency
- Genetic Linkage
- Genetic Markers
- Humans
- Karyotyping
