Ataxias on the march from Quebec to Tunisia

This publication has 9 references indexed in Scilit:

• Linkage to chromosome 13q11-12 of an autosomal recessive cerebellar ataxia in a Tunisian family
  Neurology, 2000
• Autosomal Dominant Cerebellar Ataxia Type III: Linkage in a Large British Family to a 7.6-cM Region on Chromosome 15q14-21.3
  American Journal of Human Genetics, 1999
• Location Score and Haplotype Analyses of the Locus for Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay, in Chromosome Region 13q11
  American Journal of Human Genetics, 1999
• Mapping of a New Autosomal Dominant Spinocerebellar Ataxia to Chromosome 22
  American Journal of Human Genetics, 1999
• Incidence of dominant spinocerebellar and Friedreich triplet repeats among 361 ataxia families
  Neurology, 1998
• Autosomal recessive spastic ataxia of Charlevoix–Saguenay
  Neuromuscular Disorders, 1998
• Ataxia with Isolated Vitamin E Deficiency: Heterogeneity of Mutations and Phenotypic Variability in a Large Number of Families
  American Journal of Human Genetics, 1998
• Toward Cloning of a Novel Ataxia Gene: Refined Assignment and Physical Map of the IOSCA Locus (SCA8) on 10q24
  Genomics, 1997
• Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay
  Canadian Journal of Neurological Sciences, 1978