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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 in 9p22. We confirmed more recently the close linkage to D9S15 in another set of families but found much looser...

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PMID: 2294745
PMCID: PMC1683530

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