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Phenotypic variability in friedreich ataxia: Role of the associated GAA triplet repeat expansionLaura Montermini, Massimo Pandolfo, Kenneth Morgan et al.|Annals of Neurology|1997Cited by 271
Location Score and Haplotype Analyses of the Locus for Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay, in Chromosome Region 13q11Andréa Richter, Kenneth Morgan, John D. Rioux et al.|The American Journal of Human Genetics|1999Cited by 93
Localization of a Recessive Gene for North American Indian Childhood Cirrhosis to Chromosome Region 16q22—and Identification of a Shared HaplotypeChristine Bétard, Grant A. Mitchell, Andrée Rasquin‐Weber et al.|The American Journal of Human Genetics|2000Cited by 43
Autosomal Recessive Spastic Ataxia of Charlevoix–Saguenay (ARSACS): High-Resolution Physical and Transcript Map of the Candidate Region in Chromosome Region 13q11James C. Engert, Andréa Richter, Carole Doré et al.|Genomics|1999Cited by 32