ARSACS, a spastic ataxia common in northeastern Québec, is caused by mutations in a new gene encoding an 11.5-kb ORF

Author:

Engert James C.,Bérubé Pierre,Mercier Jocelyne,Doré Carole,Lepage Pierre,Ge Bing,Bouchard Jean-Pierre,Mathieu Jean,Melançon Serge B.,Schalling Martin,Lander Eric S.,Morgan Kenneth,Hudson Thomas J.,Richter Andrea

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Reference42 articles.

1. Bouchard, J.-P. Recessive spastic ataxia of Charlevoix-Saguenay. in Handbook of Clinical Neurology 16: Hereditary Neuropathies and Spinocerebellar Degenerations (ed. de Jong, J.M.B.V.) 451–459 (Elsevier, Amsterdam, 1991).

2. Bouchard, J.P. et al>. Autosomal recessive spastic ataxia of Charlevoix-Saguenay. Neuromuscul. Disord. 8, 474– 479 (1998).

3. Richter, A. et al. Location score and haplotype analyses of the locus for autosomal recessive spastic ataxia of Charlevoix-Saguenay in chromosome region 13q11. Am. J. Hum. Genet. 64, 768– 775 (1999).

4. Charbonneau, H. & Robert, N. The French origins of the Canadian population 1608–1759. in Historical Atlas of Canada Volume I: From the Beginning to 1800 (ed. Harris, R.C.) plate 45 (University of Toronto Press, Toronto, 1987).

5. Kruglyak, L. Prospects for whole-genome linkage disequilibrium mapping of common disease genes. Nature Genet. 22, 139– 144 (1999).

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