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Revue Neurologique|January 1, 1993
[Molecular genetics and familial ataxia]M Koenig, G Sirugo, F Duclos
Proceedings of the National Academy of Sciences of the United States of America|January 1, 1993
Gene in the region of the Friedreich ataxia locus encodes a putative transmembrane protein expressed in the nervous systemF Duclos, U Boschert, G Sirugo, et al.
American Journal of Human Genetics|March 1, 1992
Friedreich ataxia in Louisiana Acadians: demonstration of a founder effect by analysis of microsatellite-generated extended haplotypesG Sirugo, B Keats, R Fujita, et al.
Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie|January 1, 1994
Mapping the Friedreich ataxia locus (FRDA) by linkage disequilibrium analysis with highly polymorphic microsatellitesG Sirugo, F Duclos, R Fujita, et al.
Human Genetics|July 1, 1992
A 530kb YAC contig tightly linked to the Friedreich ataxia locus contains five CpG clusters and a new highly polymorphic microsatelliteR Fujita, G Sirugo, F Duclos, et al.
Human Molecular Genetics|June 1, 1994
The Friedreich ataxia region: characterization of two novel genes and reduction of the critical region to 300 kbF Duclos, F Rodius, K Wrogemann, et al.
European Journal of Human Genetics : EJHG|January 1, 1993
Linkage disequilibrium analysis of Friedreich's ataxia in 140 Caucasian families: positioning of the disease locus and evaluation of allelic heterogeneityG Sirugo, S Cocozza, A Brice, et al.
American Journal of Human Genetics|December 1, 1992
Study of large inbred Friedreich ataxia families reveals a recombination between D9S15 and the disease locusS Belal, K Panayides, G Sirugo, et al.
Neurology|November 1, 1993
Friedreich's ataxia phenotype not linked to chromosome 9 and associated with selective autosomal recessive vitamin E deficiency in two inbred Tunisian familiesM Ben Hamida, S Belal, G Sirugo, et al.
The Journal of Biological Chemistry|June 6, 1998
Induction of apoptosis and inhibition of cell proliferation by survivin gene targetingG Ambrosini, C Adida, G Sirugo, et al.
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